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proteome. The turnover of some proteins is quite faster than others and the protein content of an artery may substantially vary from that of a vein. All these differences make even the simplest proteomic task of cataloging the proteome seem out of reach. To tackle this problem, priorities need to be established. Capturing the most meaningful subset of proteins among the entire proteome to generate a diagnostic tool is one such priority. Secondly, since cancer is associated with enhanced glycosylation of proteins, methods that focus on this part of proteins will also be useful. Again: multiparameter analysis best reveals a pathological state. As these technologies improve, the disease profiles should be continually related to respective gene expression changes. Due to the above-mentioned problems plasma proteomics remained challenging. However, technological advancements and continuous developments seem to result in a revival of plasma proteomics as it was shown recently by a technology called plasma proteome profiling. Due to such technologies researchers were able to investigate inflammation processes in mice, the heritability of plasma proteomes as well as to show the effect of such a common life style change like weight loss on the plasma proteome.
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throughput and sensitivity of proteomic assays, often measured as samples analyzed per day and depth of proteome coverage, respectively, have driven development of cutting-edge instrumentation and methodologies. For many cellular events, the protein concentrations do not change; rather, their function is modulated by post-translational modifications (PTM). Methods of monitoring PTM are an underdeveloped area in proteomics. Selecting a particular subset of protein for analysis substantially reduces protein complexity, making it advantageous for diagnostic purposes where blood is the starting material. Another important aspect of proteomics, yet not addressed, is that proteomics methods should focus on studying proteins in the context of the environment. The increasing use of chemical cross-linkers, introduced into living cells to fix protein-protein, protein-DNA and other interactions, may ameliorate this problem partially. The challenge is to identify suitable methods of preserving relevant interactions. Another goal for studying proteins is development of more sophisticated methods to image proteins and other molecules in living cells and real-time.
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the fluctuating state of proteome among different cell population within a small area of human tissue. This is useful for profiling the status of cellular signaling molecules, among a cross-section of tissue that includes both normal and cancerous cells. This approach is useful in monitoring the status of key factors in normal prostate epithelium and invasive prostate cancer tissues. LCM then dissects these tissue and protein lysates were arrayed onto nitrocellulose slides, which were probed with specific antibodies. This method can track all kinds of molecular events and can compare diseased and healthy tissues within the same patient enabling the development of treatment strategies and diagnosis. The ability to acquire proteomics snapshots of neighboring cell populations, using reverse-phase microarrays in conjunction with LCM has a number of applications beyond the study of tumors. The approach can provide insights into normal physiology and pathology of all the tissues and is invaluable for characterizing developmental processes and anomalies.
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antibodies are arrayed to detect their respective antigens from a sample of human blood. Another approach is the arraying of multiple protein types for the study of properties like protein-DNA, protein-protein and protein-ligand interactions. Ideally, the functional proteomic arrays would contain the entire complement of the proteins of a given organism. The first version of such arrays consisted of 5000 purified proteins from yeast deposited onto glass microscopic slides. Despite the success of first chip, it was a greater challenge for protein arrays to be implemented. Proteins are inherently much more difficult to work with than DNA. They have a broad dynamic range, are less stable than DNA and their structure is difficult to preserve on glass slides, though they are essential for most assays. The global ICAT technology has striking advantages over protein chip technologies.
1050:. Some programs will accept post-translational modifications to aid in protein identification but then ignore the modification during further protein analysis. It is important to account for these modifications since they can affect the protein's structure. In turn, computational analysis of post-translational modifications has gained the attention of the scientific community. The current post-translational modification programs are only predictive. Chemists, biologists and computer scientists are working together to create and introduce new pipelines that allow for analysis of post-translational modifications that have been experimentally identified for their effect on the protein's structure and function.
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using isotopic labeling and selective chemistries to capture the fraction of protein among the complex mixture. Secondly, the ICAT technology was used to differentiate between partially purified or purified macromolecular complexes such as large RNA polymerase II pre-initiation complex and the proteins complexed with yeast transcription factor. Thirdly, ICAT labeling was recently combined with chromatin isolation to identify and quantify chromatin-associated proteins. Finally ICAT reagents are useful for proteomic profiling of cellular organelles and specific cellular fractions.
655:
27:
379:. Proteomic analysis is highly amenable to automation and large data sets are created, which are processed by software algorithms. Filter parameters are used to reduce the number of false hits, but they cannot be completely eliminated. Scientists have expressed the need for awareness that proteomics experiments should adhere to the criteria of analytical chemistry (sufficient data quality, sanity check, validation).
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proteins to be identified by mass spectrometry. Despite the advances in 2-DE and its maturity, it has its limits as well. The central concern is the inability to resolve all the proteins within a sample, given their dramatic range in expression level and differing properties. The combination of pore size, and protein charge, size and shape can greatly determine migration rate which leads to other complications.
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that fits the active site of an enzyme, but cannot be released by the enzyme, inactivates the enzyme. This is the basis of new drug-discovery tools, which aim to find new drugs to inactivate proteins involved in disease. As genetic differences among individuals are found, researchers expect to use these techniques to develop personalized drugs that are more effective for the individual.
546:(Stål)) male accessory gland proteins (Acps) that may be transferred to females via mating, causing an increase in fecundity (i.e. birth rate) of females. To identify changes in the types of accessory gland proteins (Acps) and reproductive proteins that mated female planthoppers received from male planthoppers, researchers conducted a comparative proteomic analysis of mated
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tissue-biofluid as information channels, significant biofluid proxies can be identified and then used for the guided development of clinical diagnostics. Candidate biomarkers are then predicted based on information transfer criteria across the tissue-biofluid channels. Significant biofluid-tissue relationships can be used to prioritize clinical validation of biomarkers.
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It also contains tissue leakage proteins due to the blood circulation through different tissues in the body. The blood thus contains information on the physiological state of all tissues and, combined with its accessibility, makes the blood proteome invaluable for medical purposes. It is thought that characterizing the proteome of blood plasma is a daunting challenge.
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programs use the chemical properties of amino acids and structural properties of known proteins to predict the 3D model of sample proteins. This also allows scientists to model protein interactions on a larger scale. In addition, biomedical engineers are developing methods to factor in the flexibility of protein structures to make comparisons and predictions.
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separated by multidimensional liquid chromatography and analyzed by tandem mass spectrometry. Isotope coded affinity tag (ICAT) reagents are the widely used isotope tags. In this method, the cysteine residues of proteins get covalently attached to the ICAT reagent, thereby reducing the complexity of the mixtures omitting the non-cysteine residues.
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are currently programs available for protein identification. These programs take the peptide sequences output from mass spectrometry and microarray and return information about matching or similar proteins. This is done through algorithms implemented by the program which perform alignments with proteins from known databases such as UniProt and
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upper femtomolar range (10 M). Digital immunoassay technology has improved detection sensitivity three logs, to the attomolar range (10 M). This capability has the potential to open new advances in diagnostics and therapeutics, but such technologies have been relegated to manual procedures that are not well suited for efficient routine use.
231:. Determining which proteins are poly-ubiquitinated helps understand how protein pathways are regulated. This is, therefore, an additional legitimate "proteomic" study. Similarly, once a researcher determines which substrates are ubiquitinated by each ligase, determining the set of ligases expressed in a particular cell type is helpful.
395:. If a complex biological sample is analyzed, either a very specific antibody needs to be used in quantitative dot blot analysis (QDB), or biochemical separation then needs to be used before the detection step, as there are too many analytes in the sample to perform accurate detection and quantification.
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Characterizing the human plasma proteome has become a major goal in the proteomics arena, but it is also the most challenging proteomes of all human tissues. It contains immunoglobulin, cytokines, protein hormones, and secreted proteins indicative of infection on top of resident, hemostatic proteins.
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A number of emerging concepts have the potential to improve the current features of proteomics. Obtaining absolute quantification of proteins and monitoring post-translational modifications are the two tasks that impact the understanding of protein function in healthy and diseased cells. Further, the
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The bioorthoganal field is expanding and is driving further applications within proteomics. It is worthwhile noting the limitations and benefits. Rapid reactions can create bioconjuctions and create high concentrations with low amounts of reactants. Contrarily slow kinetic reactions like aldehyde and
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The second quantitative approach uses stable isotope tags to differentially label proteins from two different complex mixtures. Here, the proteins within a complex mixture are labeled isotopically first, and then digested to yield labeled peptides. The labeled mixtures are then combined, the peptides
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Advances in quantitative proteomics would clearly enable more in-depth analysis of cellular systems. Another research frontier is the analysis of single cells, and protein covariation across single cells which reflects biological processes such as protein complex formation, immune functions, as well
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Mass spectrometry and microarray produce peptide fragmentation information but do not give identification of specific proteins present in the original sample. Due to the lack of specific protein identification, past researchers were forced to decipher the peptide fragments themselves. However, there
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Structural proteomics includes the analysis of protein structures at large-scale. It compares protein structures and helps identify functions of newly discovered genes. The structural analysis also helps to understand that where drugs bind to proteins and also shows where proteins interact with each
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with micro array technology, to produce reverse-phase protein microarrays. In this type of microarrays, the whole collection of protein themselves are immobilized with the intent of capturing various stages of disease within an individual patient. When used with LCM, reverse phase arrays can monitor
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There are two mass spectrometry-based methods currently used for protein profiling. The more established and widespread method uses high resolution, two-dimensional electrophoresis to separate proteins from different samples in parallel, followed by selection and staining of differentially expressed
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Disease detection at the molecular level is driving the emerging revolution of early diagnosis and treatment. A challenge facing the field is that protein biomarkers for early diagnosis may be present in very low abundance. The lower limit of detection with conventional immunoassay technology is the
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Immunoassays can also be carried out using recombinantly generated immunoglobulin derivatives or synthetically designed protein scaffolds that are selected for high antigen specificity. Such binders include single domain antibody fragments (Nanobodies), designed ankyrin repeat proteins (DARPins) and
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Because protein phosphorylation is one of the most studied protein modifications, many "proteomic" efforts are geared to determining the set of phosphorylated proteins in a particular cell or tissue-type under particular circumstances. This alerts the scientist to the signaling pathways that may be
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at a larger scale. It helps identify main proteins in a particular sample, and those proteins differentially expressed in related samples—such as diseased vs. healthy tissue. If a protein is found only in a diseased sample then it can be a useful drug target or diagnostic marker. Proteins with the
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information to identify proteins associated with a disease, which computer software can then use as targets for new drugs. For example, if a certain protein is implicated in a disease, its 3D structure provides the information to design drugs to interfere with the action of the protein. A molecule
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Balancing the use of mass spectrometers in proteomics and in medicine is the use of protein micro arrays. The aim behind protein micro arrays is to print thousands of protein detecting features for the interrogation of biological samples. Antibody arrays are an example in which a host of different
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One example of the use of bioinformatics and the use of computational methods is the study of protein biomarkers. Computational predictive models have shown that extensive and diverse feto-maternal protein trafficking occurs during pregnancy and can be readily detected non-invasively in maternal
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Understanding the proteome, the structure and function of each protein and the complexities of protein–protein interactions are critical for developing the most effective diagnostic techniques and disease treatments in the future. For example, proteomics is highly useful in the identification of
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using stable isotopic tagging is an increasingly useful tool in modern development. Firstly, chemical reactions have been used to introduce tags into specific sites or proteins for the purpose of probing specific protein functionalities. The isolation of phosphorylated peptides has been achieved
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While protein detection with antibodies is still very common in molecular biology, other methods have been developed as well, that do not rely on an antibody. These methods offer various advantages, for instance they often are able to determine the sequence of a protein or peptide, they may have
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for a specific cancer subtype is sought, the proteomics scientist might elect to study multiple blood serum samples from multiple cancer patients to minimise confounding factors and account for experimental noise. Thus, complicated experimental designs are sometimes necessary to account for the
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The depth of the plasma proteome encompasses a dynamic range of more than 10 between the highest abundant protein (albumin) and the lowest (some cytokines) and is thought to be one of the main challenges for proteomics. Temporal and spatial dynamics further complicate the study of human plasma
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is a leading technique, solving difficulties with crystallization (in X-ray crystallography) and conformational ambiguity (in NMR); resolution was 2.2Å as of 2015. Now, through bioinformatics, there are computer programs that can in some cases predict and model the structure of proteins. These
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Proteomics has steadily gained momentum over the past decade with the evolution of several approaches. Few of these are new, and others build on traditional methods. Mass spectrometry-based methods, affinity proteomics, and micro arrays are the most common technologies for large-scale study of
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of tryptic peptides. Although early large-scale shotgun proteomics analyses showed considerable variability between laboratories, presumably due in part to technical and experimental differences between laboratories, reproducibility has been improved in more recent mass spectrometry analysis,
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discovery, integrating biofluid and tissue information. This new approach takes advantage of functional synergy between certain biofluids and tissues with the potential for clinically significant findings not possible if tissues and biofluids were considered individually. By conceptualizing
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Specific biomolecules that are capable of being metabolized in cells or tissues are inserted into proteins or glycans. The molecule will have an affinity tag, modifying the protein allowing it to be detected. Azidohomoalanine (AHA) utilizes this affinity tag via incorporation with Met-t-RNA
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and microarray. It would often take weeks or months to analyze the data and perform comparisons by hand. For this reason, biologists and chemists are collaborating with computer scientists and mathematicians to create programs and pipeline to computationally analyze the protein data. Using
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Affinity proteomics uses antibodies or other affinity reagents (such as oligonucleotide-based aptamers) as protein-specific detection probes. Currently this method can interrogate several thousand proteins, typically from biofluids such as plasma, serum or cerebrospinal fluid (CSF). A key
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There are many approaches to characterizing the human proteome, which is estimated to contain between 20,000 and 25,000 non-redundant proteins. The number of unique protein species likely will increase by between 50,000 and 500,000 due to RNA splicing and proteolysis events, and when
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Not only does the translation from mRNA cause differences, but many proteins also are subjected to a wide variety of chemical modifications after translation. The most common and widely studied post-translational modifications include phosphorylation and glycosylation. Many of these
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is not always translated into protein, and the amount of protein produced for a given amount of mRNA depends on the gene it is transcribed from and on the cell's physiological state. Proteomics confirms the presence of the protein and provides a direct measure of its quantity.
628:. In this approach, increased throughput and sensitivity is achieved by avoiding the need for tandem mass spectrometry, and making use of precisely determined separation time information and highly accurate mass determinations for peptide and protein identifications.
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candidate biomarkers (proteins in body fluids that are of value for diagnosis), identification of the bacterial antigens that are targeted by the immune response, and identification of possible immunohistochemistry markers of infectious or neoplastic diseases.
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responses to these perturbations results in functional changes to the proteome implicated in response to the stimulus. Therefore, describing and quantifying proteome-wide changes in protein abundance is crucial towards understanding biological phenomenon more
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differentiator for this technology is the ability to analyze hundreds or thousands of samples in a reasonable timeframe (a matter of days or weeks); mass spectrometry-based methods are not scalable to this level of sample throughput for proteomics analyses.
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is the entire set of proteins produced or modified by an organism or system. Proteomics enables the identification of ever-increasing numbers of proteins. This varies with time and distinct requirements, or stresses, that a cell or organism undergoes.
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An interesting use of proteomics is using specific protein biomarkers to diagnose disease. A number of techniques allow to test for proteins produced during a particular disease, which helps to diagnose the disease quickly. Techniques include
145:, proteomics is the next step in the study of biological systems. It is more complicated than genomics because an organism's genome is more or less constant, whereas proteomes differ from cell to cell and from time to time. Distinct genes are
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Rozanova, Svitlana; Barkovits, Katalin; Nikolov, Miroslav; Schmidt, Carla; Urlaub, Henning; Marcus, Katrin (2021), Marcus, Katrin; Eisenacher, Martin; Sitek, Barbara (eds.), "Quantitative Mass
Spectrometry-Based Proteomics: An Overview",
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forms the 3D configuration of the protein. Understanding the protein's structure aids in the identification of the protein's interactions and function. It used to be that the 3D structure of proteins could only be determined using
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Comparative proteomic analysis may reveal the role of proteins in complex biological systems, including reproduction. For example, treatment with the insecticide triazophos causes an increase in the content of brown planthopper
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Fluorescence two-dimensional differential gel electrophoresis (2-D DIGE) may be used to quantify variation in the 2-D DIGE process and establish statistically valid thresholds for assigning quantitative changes between samples.
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Arora PS, Yamagiwa H, Srivastava A, Bolander ME, Sarkar G (2005). "Comparative evaluation of two two-dimensional gel electrophoresis image analysis software applications using synovial fluids from patients with joint disease".
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has defined a biomarker as "a characteristic that is objectively measured and evaluated as an indicator of normal biological processes, pathogenic processes, or pharmacologic responses to a therapeutic intervention."
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Peng J, Elias JE, Thoreen CC, Licklider LJ, Gygi SP (2003). "Evaluation of multidimensional chromatography coupled with tandem mass spectrometry (LC/LC-MS/MS) for large-scale protein analysis: the yeast proteome".
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Wang LP, Shen J, Ge LQ, Wu JC, Yang GQ, Jahn GC (November 2010). "Insecticide-induced increase in the protein content of male accessory glands and its effect on the fecundity of females in the brown planthopper,
437:, they are known as phospho-specific antibodies. Also, there are antibodies specific to other modifications. These may be used to determine the set of proteins that have undergone the modification of interest.
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Klopfleisch R, Klose P, Weise C, Bondzio A, Multhaup G, Einspanier R, Gruber AD (December 2010). "Proteome of metastatic canine mammary carcinomas: similarities to and differences from human breast cancer".
963:. Parallel analysis of the genome and the proteome facilitates discovery of post-translational modifications and proteolytic events, especially when comparing multiple species (comparative proteogenomics).
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Huffman RG, Leduc A, Wichmann C, di Gioia M, Borriello F, Specht H, et al. (2022-03-18). "Prioritized single-cell proteomics reveals molecular and functional polarization across primary macrophages".
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Tonge R, Shaw J, Middleton B, Rowlinson R, Rayner S, Young J, et al. (March 2001). "Validation and development of fluorescence two-dimensional differential gel electrophoresis proteomics technology".
3169:"Proteomic analysis of differentially expressed protein in hemocytes of wild giant freshwater prawn Macrobrachium rosenbergii infected with infectious hypodermal and hematopoietic necrosis virus (IHHNV)"
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Several hybrid technologies use antibody-based purification of individual analytes and then perform mass spectrometric analysis for identification and quantification. Examples of these methods are the
1071:. Such work shows that the fetal proteins detected in pregnant woman's blood originate from a diverse group of tissues and organs from the developing fetus. The proteomic networks contain many
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1162:. Similar datasets in other cell types, tissue types, and species, particularly using deep shotgun mass spectrometry, will be an immensely important resource for research in fields like
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journals are more focused on the large-scale analysis of whole proteomes or at least large sets of proteins. Some relevant proteomics journals are listed below (with their publishers).
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Ge LQ, Cheng Y, Wu JC, Jahn GC (October 2011). "Proteomic analysis of insecticide triazophos-induced mating-responsive proteins of
Nilaparvata lugens Stål (Hemiptera: Delphacidae)".
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studies. These are among the most common tools used by molecular biologists today. There are several specific techniques and protocols that use antibodies for protein detection. The
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The first studies of proteins that could be regarded as proteomics began in 1974, after the introduction of the two-dimensional gel and mapping of the proteins from the bacterium
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Wasinger VC, Cordwell SJ, Cerpa-Poljak A, Yan JX, Gooley AA, Wilkins MR, et al. (July 1995). "Progress with gene-product mapping of the
Mollicutes: Mycoplasma genitalium".
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is subjected to multiple steps of chemical degradation to resolve its sequence. These early methods have mostly been supplanted by technologies that offer higher throughput.
267:. Some proteins undergo all these modifications, often in time-dependent combinations. This illustrates the potential complexity of studying protein structure and function.
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Eichelbaum K, Winter M, Berriel Diaz M, Herzig S, Krijgsveld J (October 2012). "Selective enrichment of newly synthesized proteins for quantitative secretome analysis".
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One major development to come from the study of human genes and proteins has been the identification of potential new drugs for the treatment of disease. This relies on
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have revealed applications in protein analysis. The extension of using organic molecules to observe their reaction with proteins reveals extensive methods to tag them.
718:. However, using ketones and aldehydes as bioorthogonal reporters revealed slow kinetics indicating that while effective for labeling, the concentration must be high.
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Ceciliani F, Eckersall D, Burchmore R, Lecchi C (March 2014). "Proteomics in veterinary medicine: applications and trends in disease pathogenesis and diagnostics".
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Ceciliani F, Eckersall D, Burchmore R, Lecchi C (March 2014). "Proteomics in veterinary medicine: applications and trends in disease pathogenesis and diagnostics".
529:, developed by Randall Nelson in 1995, and the SISCAPA (Stable Isotope Standard Capture with Anti-Peptide Antibodies) method, introduced by Leigh Anderson in 2004.
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Ketone and aldehyde mechanism with cell surface labeling. Staudinger ligations and their interaction with azide groups for labeling are shown in the second figure.
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bioinformatics resource portal. The applications of bioinformatics-based proteomics include medicine, disease diagnosis, biomarker identification, and many more.
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Proteomics is also used to reveal complex plant-insect interactions that help identify candidate genes involved in the defensive response of plants to herbivory.
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Reumann S (May 2011). "Toward a definition of the complete proteome of plant peroxisomes: Where experimental proteomics must be complemented by bioinformatics".
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that are proxies for development and illustrate the potential clinical application of this technology as a way to monitor normal and abnormal fetal development.
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In addition, the first promising attempts to decipher the proteome of animal tumors have recently been reported. This method was used as a functional method in
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Interaction proteomics is the analysis of protein interactions from scales of binary interactions to proteome- or network-wide. Most proteins function via
101:. Indeed, mass spectrometry is the most powerful method for analysis of proteomes, both in large samples composed of millions of cells and in single cells.
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3682:"Proteome Analysis of Rice (Oryza sativa L.) Mutants Reveals Differentially Induced Proteins during Brown Planthopper (Nilaparvata lugens) Infestation"
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synthetase to incorporate into proteins. This has allowed AHA to assist in determine the identity of newly synthesized proteins created in response to
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This is a promising and newer microarray application for the diagnosis, study and treatment of complex diseases such as cancer. The technology merges
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Therefore, a "proteomics" study may become complex very quickly, even if the topic of study is restricted. In more ambitious settings, such as when a
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Weston AD, Hood L (2004). "Systems biology, proteomics, and the future of health care: toward predictive, preventative, and personalized medicine".
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Washburn MP, Wolters D, Yates JR (March 2001). "Large-scale analysis of the yeast proteome by multidimensional protein identification technology".
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separation. More recently, on-line methods have been developed where individual peptides (in bottom-up proteomics approaches) are separated using
83:. It covers the exploration of proteomes from the overall level of protein composition, structure, and activity, and is an important component of
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techniques, researchers are capable of faster analysis and data storage. A good place to find lists of current programs and databases is on the
212:—causes a protein to become a target for binding or interacting with a distinct set of other proteins that recognize the phosphorylated domain.
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whole blood. This computational approach circumvented a major limitation, the abundance of maternal proteins interfering with the detection of
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provides quantitative protein expression data for ~200 proteins in over 4,000 tumor samples with matched transcriptomic and genomic data from
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may be used for detection and quantification of individual proteins, where in an initial step, a complex protein mixture is separated using
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shows increased reproducibility and repeatability compared with shotgun methods, although at the expense of data density and effectiveness.
291:. Further increasing proteome complexity, as mentioned, most proteins are able to undergo a wide range of post-translational modifications.
79:
Proteomics is an interdisciplinary domain that has benefited greatly from the genetic information of various genome projects, including the
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1585:"Comprehensive Proteomic Analysis of Mesenchymal Stem Cell Exosomes Reveals Modulation of Angiogenesis via Nuclear Factor-KappaB Signaling"
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Jensen ON (February 2004). "Modification-specific proteomics: characterization of post-translational modifications by mass spectrometry".
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post-translational modification also are considered, the total number of unique human proteins is estimated to range in the low millions.
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Biomarkers
Definitions Working Group (March 2001). "Biomarkers and surrogate endpoints: preferred definitions and conceptual framework".
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and secretion pathways using proteomic approaches, has recently emerged as an important tool for the discovery of biomarkers of disease.
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In the past this phenomenon was assessed by RNA analysis, which was found to lack correlation with protein content. It is now known that
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506:
2561:"Spectral quality overrides software score-A brief tutorial on the analysis of peptide fragmentation data for mass spectrometry laymen"
1063:, to fetal proteomic analysis of maternal blood. Computational models can use fetal gene transcripts previously identified in maternal
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477:-based techniques, a development that was made possible by the discovery of "soft ionization" methods developed in the 1980s, such as
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that profoundly affect their activities; for example, some proteins are not active until they become phosphorylated. Methods such as
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Rakwal R, Komatsu S (July 2000). "Role of jasmonate in the rice (Oryza sativa L.) self-defense mechanism using proteome analysis".
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Mechanisms showing how AHA labels onto proteins and where biotin-FLAG-alkyne tags mark the amino acid. Hand Drawn via Sigma
Aldrich
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Stoevesandt O, Taussig MJ (August 2012). "Affinity proteomics: the role of specific binding reagents in human proteome analysis".
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2778:"The Simoa HD-1 Analyzer: A Novel Fully Automated Digital Immunoassay Analyzer with Single-Molecule Sensitivity and Multiplexing"
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is also informative). Proteome-wide analysis of protein interactions, and integration of these interaction patterns into larger
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For the analysis of complex biological samples, a reduction of sample complexity is required. This may be performed off-line by
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many proteins form complexes with other proteins or RNA molecules, and only function in the presence of these other molecules.
4196:"Whole proteome analysis of post-translational modifications: applications of mass-spectrometry for proteogenomic annotation"
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as cell cycle and priming of cancer cells for drug resistance
Biological systems are subject to a variety of perturbations (
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higher throughput than antibody-based, and they sometimes can identify and quantify proteins for which no antibody exists.
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1989:"Investigating the correspondence between transcriptomic and proteomic expression profiles using coupled cluster models"
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other. This understanding is achieved using different technologies such as X-ray crystallography and NMR spectroscopy.
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5053:"Large-scale inference of protein tissue origin in gram-positive sepsis plasma using quantitative targeted proteomics"
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generally denotes the large-scale experimental analysis of proteins and proteomes, but often refers specifically to
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specific to that modification. For example, some antibodies only recognize certain proteins when they are tyrosine-
370:
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Domon B, Aebersold R (July 2010). "Options and considerations when selecting a quantitative proteomics strategy".
2367:"Repeatability and reproducibility in proteomic identifications by liquid chromatography-tandem mass spectrometry"
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Anderson NL, Anderson NG (August 1998). "Proteome and proteomics: new technologies, new concepts, and new words".
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produced in abundance may be degraded rapidly or translated inefficiently, resulting in a small amount of protein.
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same or similar expression profiles may also be functionally related. There are technologies such as 2D-PAGE and
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In proteomics, there are multiple methods to study proteins. Generally, proteins may be detected by using either
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A cell may make different sets of proteins at different times or under different conditions, for example during
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in different cell types, which means that even the basic set of proteins produced in a cell must be identified.
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2510:"Proteomics Is Analytical Chemistry: Fitness-for-Purpose in the Application of Top-Down and Bottom-Up Analyses"
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has been established as the major unbiased approach for identifying new peroxisomal proteins on a large scale.
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4245:"Comparative proteogenomics: combining mass spectrometry and comparative genomics to analyze multiple genomes"
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Numerous journals are dedicated to the field of proteomics and related areas. Note that journals dealing with
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4489:"High-throughput discovery and characterization of fetal protein trafficking in the blood of pregnant women"
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Sabidó E, Selevsek N, Aebersold R (August 2012). "Mass spectrometry-based proteomics for systems biology".
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Dhingra V, Gupta M, Andacht T, Fu ZF (August 2005). "New frontiers in proteomics research: a perspective".
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Blackstock WP, Weir MP (March 1999). "Proteomics: quantitative and physical mapping of cellular proteins".
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Bensimon A, Heck AJ, Aebersold R (7 July 2012). "Mass spectrometry-based proteomics and network biology".
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1021:
805:
700:
5108:
Geyer PE, Wewer
Albrechtsen NJ, Tyanova S, Grassl N, Iepsen EW, Lundgren J, et al. (December 2016).
6363:
6317:
5736:
5711:
5691:
1242:
1167:
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1026:
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2141:
Srinivas PR, Verma M, Zhao Y, Srivastava S (August 2002). "Proteomics for cancer biomarker discovery".
1734:"Initial recommendations for performing, benchmarking and reporting single-cell proteomics experiments"
1840:"[48] Two-dimensional polyacrylamide gel electrophoresis for separation of ribosomal proteins"
6123:
6108:
5956:
5766:
5716:
5064:
4392:
2617:
2230:
1926:
1308:
1259:
1254:
1079:
1072:
864:
801:
786:
490:
340:
126:
94:
80:
20:
4104:"Increased expression of BRCA2 and RAD51 in lymph node metastases of canine mammary adenocarcinomas"
3241:
2653:"Selection and identification of single domain antibody fragments from camel heavy-chain antibodies"
1583:
Anderson JD, Johansson HJ, Graham CS, Vesterlund M, Pham MT, Bramlett CS, et al. (March 2016).
6598:
6551:
6333:
6307:
6165:
6152:
6113:
5871:
5741:
3645:
Wu J, Baldwin IT (2010). "New insights into plant responses to the attack from insect herbivores".
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Stumpp MT, Binz HK, Amstutz P (August 2008). "DARPins: a new generation of protein therapeutics".
6567:
6287:
6098:
6032:
5986:
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5951:
5776:
5771:
5585:
5314:
5248:
Belhajjame K, Embury SM, Fan H, Goble CA, Hermjakob H, Hubbard SJ, et al. (September 2005).
5236:
4806:
4578:
4440:"Vienna-PTM web server: a toolkit for MD simulations of protein post-translational modifications"
4176:
4133:
4084:
4031:
3846:
3627:
3459:
3416:
3368:
3306:
3034:
2918:
2682:
2590:
2439:
2347:
2123:
1895:
1771:
1530:
1378:
1358:
1323:
868:
848:
821:
715:
418:(ELISA) has been used for decades to detect and quantitatively measure proteins in samples. The
365:
2365:
Tabb DL, Vega-Montoto L, Rudnick PA, Variyath AM, Ham AJ, Bunk DM, et al. (February 2010).
1839:
5051:
Malmström E, Kilsgård O, Hauri S, Smeds E, Herwald H, Malmström L, Malmström J (January 2016).
733:. This reaction has already been used to label other biomolecules in living cells and animals.
6603:
6524:
6498:
6338:
6147:
6061:
5971:
5851:
5706:
5509:
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5433:
5413:
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5350:
5342:
5331:
5306:
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5228:
5188:
5139:
5090:
5033:
4982:
4947:
4906:
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4723:
4674:
4625:
4566:
4556:
4518:
4469:
4420:
4361:
4274:
4225:
4168:
4125:
4076:
4023:
3988:
3922:
3884:
3838:
3803:
3793:
3762:
3713:
3662:
3619:
3584:
3543:
3494:
3451:
3408:
3360:
3350:
3298:
3288:
3254:
3198:
3149:
3110:
3075:
3026:
2988:
2910:
2842:
2834:
2799:
2758:
2717:
2674:
2633:
2582:
2541:
2490:
2431:
2396:
2339:
2304:
2258:
2199:
2150:
2115:
2072:
2053:
2018:
1944:
1887:
1846:, Nucleic Acids and Protein Synthesis Part F, vol. 30, Academic Press, pp. 497–505,
1820:
1763:
1714:
1665:
1614:
1565:
1522:
1438:
1353:
1046:
Most programs available for protein analysis are not written for proteins that have undergone
981:
956:
940:
932:
889:
592:
550:
females. The results indicated that these proteins participate in the reproductive process of
474:
463:
392:
329:
98:
34:
5268:
3821:
Visser NF, Heck AJ (June 2008). "Surface plasmon resonance mass spectrometry in proteomics".
1130:, on the level of the entire system. In this way, proteomics can be seen as complementary to
737:
ketone condensation while effective require a high concentration making it cost inefficient.
6262:
6257:
5696:
5499:
5382:
5374:
5296:
5288:
5220:
5178:
5170:
5129:
5121:
5080:
5072:
5023:
5013:
4974:
4937:
4926:"The clinical plasma proteome: a survey of clinical assays for proteins in plasma and serum"
4896:
4888:
4847:
4837:
4798:
4764:
4754:
4713:
4705:
4664:
4656:
4617:
4548:
4508:
4500:
4459:
4451:
4410:
4400:
4351:
4341:
4264:
4256:
4215:
4207:
4160:
4115:
4066:
4058:
4015:
3978:
3970:
3914:
3876:
3830:
3785:
3752:
3744:
3703:
3693:
3680:
Sangha JS, Chen YH, Kaur J, Khan W, Abduljaleel Z, Alanazi MS, et al. (February 2013).
3654:
3611:
3574:
3533:
3525:
3486:
3443:
3400:
3340:
3332:
3278:
3277:, Methods in Molecular Biology, vol. 2228, New York, NY: Springer US, pp. 85–116,
3246:
3188:
3180:
3141:
3102:
3065:
3018:
2980:
2950:
2902:
2826:
2789:
2776:
Wilson DH, Rissin DM, Kan CW, Fournier DR, Piech T, Campbell TG, et al. (August 2016).
2748:
2709:
2664:
2625:
2572:
2531:
2521:
2480:
2470:
2459:"A Critical Review of Bottom-Up Proteomics: The Good, the Bad, and the Future of this Field"
2423:
2386:
2378:
2331:
2296:
2248:
2238:
2189:
2181:
2105:
2045:
2008:
2000:
1934:
1879:
1847:
1810:
1802:
1753:
1745:
1704:
1696:
1655:
1645:
1604:
1596:
1557:
1514:
1333:
1030:
692:
621:
620:
Another quantitative approach is the accurate mass and time (AMT) tag approach developed by
111:
4194:
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2817:
Nelson RW, Krone JR, Bieber AL, Williams P (April 1995). "Mass spectrometric immunoassay".
356:. One major factor affecting reproducibility in proteomics experiments is the simultaneous
121:
is a blend of the words "protein" and "genome". It was coined in 1994 by then-Ph.D student
52:
of all living organisms, with many functions such as the formation of structural fibers of
6529:
6277:
6267:
6252:
6188:
5981:
5946:
5535:
5028:
4590:
3880:
3345:
3331:, Methods in Molecular Biology, vol. 893, Totowa, NJ: Humana Press, pp. 85–100,
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142:
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5068:
4605:
4396:
4243:
Gupta N, Benhamida J, Bhargava V, Goodman D, Kain E, Kerman I, et al. (July 2008).
3658:
3324:
2621:
2234:
1930:
1758:
1733:
980:
Much proteomics data is collected with the help of high throughput technologies such as
6608:
6434:
6272:
6175:
6118:
5836:
5646:
5387:
5362:
5183:
5158:
5134:
5109:
5085:
5052:
4901:
4876:
4852:
4825:
4769:
4742:
4718:
4693:
4692:
Derks J, Leduc A, Wallmann G, Huffman RG, Willetts M, Khan S, et al. (July 2022).
4669:
4644:
4513:
4488:
4464:
4439:
4415:
4380:
4356:
4329:
4269:
4244:
4220:
4195:
3983:
3958:
3757:
3732:
3708:
3681:
3538:
3513:
3193:
3168:
2536:
2509:
2485:
2458:
2391:
2366:
2253:
2218:
2013:
1988:
1815:
1790:
1709:
1684:
1660:
1633:
1609:
1584:
1363:
1280:
1110:
986:
952:
856:
517:; the direct coupling of separation and analysis explains the term "on-line" analysis.
434:
288:
244:
227:
is a small protein that may be affixed to certain protein substrates by enzymes called
189:
5504:
5487:
5157:
Liu Y, Buil A, Collins BC, Gillet LC, Blum LC, Cheng LY, et al. (February 2015).
5110:"Proteomics reveals the effects of sustained weight loss on the human plasma proteome"
2669:
2652:
1732:
Gatto L, Aebersold R, Cox J, Demichev V, Derks J, Emmott E, et al. (March 2023).
1561:
493:
workflows where often additional separation is performed before analysis (see below).
6592:
6247:
6193:
6157:
5916:
5811:
5701:
5676:
5671:
5530:
5406:
4810:
3310:
2594:
2194:
2169:
1987:
Rogers S, Girolami M, Kolch W, Waters KM, Liu T, Thrall B, Wiley HS (December 2008).
1851:
1775:
1060:
837:
264:
256:
153:
53:
49:
5488:"Biomarkers of cardiovascular disease: molecular basis and practical considerations"
5318:
5240:
4180:
4137:
4088:
3850:
3631:
3420:
3372:
3038:
2922:
2443:
2351:
2092:
Olsen JV, Blagoev B, Gnad F, Macek B, Kumar C, Mortensen P, Mann M (November 2006).
2004:
1534:
307:
Proteomics gives a different level of understanding than genomics for many reasons:
6237:
6198:
6130:
5961:
5941:
5906:
5901:
5891:
5886:
5866:
5846:
5756:
5726:
5686:
5666:
5656:
5636:
5631:
5626:
5621:
3748:
3463:
2686:
2127:
2094:"Global, in vivo, and site-specific phosphorylation dynamics in signaling networks"
1899:
1433:
1143:
920:
419:
411:
407:
4035:
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Arbabi
Ghahroudi M, Desmyter A, Wyns L, Hamers R, Muyldermans S (September 1997).
2049:
5469:
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Research: New Frontiers in Functional Genomics (Principles and Practice)
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Lang K, Chin JW (January 2014). "Bioorthogonal reactions for labeling proteins".
3323:
Nikolov, Miroslav; Schmidt, Carla; Urlaub, Henning (2012), Marcus, Katrin (ed.),
2954:
2753:
2736:
2713:
6210:
6142:
6011:
6006:
5976:
5931:
5876:
5816:
5801:
5796:
5761:
5721:
5611:
5601:
5596:
4978:
4660:
3789:
3336:
3283:
3184:
1456:
1373:
1139:
1064:
936:
813:
790:
252:
248:
5018:
5001:
4842:
4709:
4552:
4330:"A local average distance descriptor for flexible protein structure comparison"
4120:
4103:
3579:
3562:
3529:
3106:
3070:
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2737:"Aptamers: an emerging class of molecules that rival antibodies in diagnostics"
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Duncan MW (June 2012). "Good mass spectrometry and its place in good science".
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Proceedings of the
National Academy of Sciences of the United States of America
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1274:
6242:
6232:
6227:
5996:
5991:
5921:
5861:
5826:
5821:
5791:
5751:
5731:
5661:
5641:
5224:
4802:
1462:
1348:
1270:
1102:
403:
361:
284:
61:
5292:
4965:
Anderson L (July 2014). "Six decades searching for meaning in the proteome".
4629:
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4164:
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3834:
2794:
2777:
2526:
2475:
1883:
6354:
Matrix-assisted laser desorption ionization-time of flight mass spectrometer
6222:
5911:
5896:
5881:
5831:
5806:
5159:"Quantitative variability of 342 plasma proteins in a human twin population"
4875:
Li J, Lu Y, Akbani R, Ju Z, Roebuck PL, Liu W, et al. (November 2013).
4379:
Petrov D, Margreitter C, Grandits M, Oostenbrink C, Zagrovic B (July 2013).
4346:
4019:
2243:
1518:
1403:
1179:
1171:
1151:
901:
847:
Knowledge of protein-protein interactions is especially useful in regard to
260:
224:
197:
5513:
5396:
5310:
5232:
5192:
5143:
5094:
5037:
4986:
4951:
4910:
4861:
4778:
4727:
4678:
4570:
4522:
4504:
4473:
4424:
4365:
4278:
4229:
4172:
4129:
4080:
4027:
3992:
3926:
3888:
3842:
3807:
3766:
3717:
3666:
3623:
3588:
3547:
3498:
3455:
3412:
3364:
3302:
3258:
3202:
3153:
3114:
3079:
3030:
3022:
2992:
2914:
2846:
2803:
2762:
2721:
2637:
2586:
2545:
2494:
2435:
2400:
2343:
2308:
2262:
2203:
2154:
2119:
2057:
2022:
1824:
1767:
1718:
1669:
1618:
1569:
769:
provides numerous tools and techniques to detect protein targets of drugs.
6446:
5174:
5125:
4487:
Maron JL, Alterovitz G, Ramoni M, Johnson KL, Bianchi DW (December 2009).
4260:
3616:
10.1002/1522-2683(20000701)21:12<2492::AID-ELPS2492>3.0.CO;2-2
2678:
2185:
1948:
1891:
1526:
6084:
6001:
5926:
5856:
5786:
5781:
5606:
5000:
Geyer PE, Kulak NA, Pichler G, Holdt LM, Teupser D, Mann M (March 2016).
4826:"Exploring functional protein covariation across single cells using nPOP"
4455:
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Hathout Y (April 2007). "Approaches to the study of the cell secretome".
3698:
1313:
1247:
1175:
1131:
755:
711:
502:
430:
423:
388:
205:
172:
post-translational modifications are critical to the protein's function.
138:
72:
65:
5076:
2830:
311:
the level of transcription of a gene gives only a rough estimate of its
6183:
6016:
5746:
5616:
5301:
4892:
4211:
4071:
2861:"SISCAPA, Stable Isotope Standard Capture with Anti-Peptide Antibodies"
1634:"The Human Genome Project: big science transforms biology and medicine"
1467:
1398:
1205:
1068:
1006:
to predict what proteins are in the sample with a degree of certainty.
1003:
467:
360:
of many more peptides than mass spectrometers can measure. This causes
357:
209:
185:
45:
5554:
4743:"Learning from natural variation across the proteomes of single cells"
3490:
3404:
3250:
3145:
2984:
2838:
2382:
2300:
1700:
1600:
192:. The addition of a phosphate to particular amino acids—most commonly
5681:
5549:
5378:
5257:. Proceedings of the UK e-Science All Hands Meeting. Nottingham, UK.
4541:"System-wide peripheral biomarker discovery using information theory"
3447:
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Alinejad T, Bin KQ, Vejayan J, Othman RY, Bhassu S (September 2015).
2629:
2577:
2560:
2427:
1939:
1914:
1163:
1127:
990:
751:
707:
201:
193:
2907:
10.1002/1615-9861(200103)1:3<377::AID-PROT377>3.0.CO;2-6
2219:"Quantification of protein half-lives in the budding yeast proteome"
349:
protein degradation rate plays an important role in protein content.
6520:
Stable isotope labeling by/with amino acids in cell culture (SILAC)
1459:—The collaborative, 3D encyclopedia of proteins and other molecules
1150:
approaches in integrative analyses attempting to define biological
406:
to particular proteins, or their modified forms, have been used in
129:, which founded the first dedicated proteomics laboratory in 1995.
4824:
Leduc A, Huffman RG, Cantlon J, Khan S, Slavov N (December 2022).
2335:
1650:
1147:
722:
596:
426:
and then the protein of interest is identified using an antibody.
31:
25:
2217:
Belle A, Tanay A, Bitincka L, Shamir R, O'Shea EK (August 2006).
5408:
Proteomics in Practice: A Laboratory Manual of Proteome Analysis
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An information-theoretic framework has also been introduced for
316:
6450:
6057:
5558:
3784:. Methods in Molecular Biology. Vol. 800. pp. 33–53.
3733:"How chemoproteomics can enable drug discovery and development"
56:, enzymatic digestion of food, or synthesis and replication of
5363:"Platelet genomics and proteomics in human health and disease"
5002:"Plasma Proteome Profiling to Assess Human Health and Disease"
4694:"Increasing the throughput of sensitive proteomics by plexDIA"
3780:
de Mol NJ (2012). "Surface Plasmon Resonance for Proteomics".
3563:"Redefining clinical trials: the age of personalized medicine"
3325:"Quantitative Mass Spectrometry-Based Proteomics: An Overview"
1962:
57:
4310:
1683:
Zhang Y, Fonslow BR, Shan B, Baek MC, Yates JR (April 2013).
714:
condensations show that they are best suited for in vitro or
339:
many transcripts give rise to more than one protein, through
6535:
Isobaric tags for relative and absolute quantitation (iTRAQ)
6053:
5467:
Wilkins MR, Williams KL, Appel RD, Hochstrasser DF (1997).
4292:
462:
One of the earliest methods for protein analysis has been
5251:
Proteome Data Integration: Characteristics and Challenges
4539:
Alterovitz G, Xiang M, Liu J, Chang A, Ramoni MF (2008).
3222:
3220:
3218:
3216:
3214:
3212:
2170:"Correlation between protein and mRNA abundance in yeast"
1209:
are usually more focused on structure and function while
721:
Certain proteins can be detected via their reactivity to
4877:"TCPA: a resource for cancer functional proteomics data"
2168:
Gygi SP, Rochon Y, Franza BR, Aebersold R (March 1999).
1067:
to create a comprehensive proteomic network of the term
3938:
3936:
3054:"Antibody-based proteomics for human tissue profiling"
5328:
Introduction to proteomics: tools for the new biology
729:
can bear azide groups which react with phosphines in
1054:
Computational methods in studying protein biomarkers
976:
Bioinformatics for proteomics (proteome informatics)
6560:
6507:
6377:
6326:
6286:
6174:
6091:
6025:
4606:"Instrumentation at the Leading Edge of Proteomics"
1791:"Single-cell protein analysis by mass spectrometry"
872:
479:
matrix-assisted laser desorption/ionization (MALDI)
336:
are used to study post-translational modifications.
5405:
4534:
4532:
1969:. New South Wales, Australia: Macquarie University
1963:"APAF - The Australian Proteome Analysis Facility"
1685:"Protein analysis by shotgun/bottom-up proteomics"
695:represent new growing technologies in proteomics.
429:Modified proteins may be studied by developing an
271:Distinct proteins are made under distinct settings
4438:Margreitter C, Petrov D, Zagrovic B (July 2013).
68:that send important signals throughout the body.
3862:
3860:
2966:
2964:
601:LCQ Mass Spectrometer used in mass spectrometry.
399:Protein detection with antibodies (immunoassays)
343:or alternative post-translational modifications.
5430:Principles Of Proteomics (Advanced Text Series)
4328:Wang HW, Chu CH, Wang WC, Pai TW (April 2014).
3126:
3124:
883:Expression proteomics includes the analysis of
781:, and one goal of interaction proteomics is to
60:. In addition, other kinds of proteins include
3900:
3898:
391:(immunoassays), electrophoretic separation or
303:Limitations of genomics and proteomics studies
247:, proteins may be subjected to (among others)
6462:
6069:
5570:
1428:National Center for Biotechnology Information
800:. While the most traditional method is yeast
671:Protein Detection via Bioorthogonal Chemistry
322:as mentioned above, many proteins experience
64:that protect an organism from infection, and
8:
3004:
3002:
703:and to identify proteins secreted by cells.
369:particularly on the protein level. Notably,
6349:Matrix-assisted laser desorption ionization
3686:International Journal of Molecular Sciences
773:Interaction proteomics and protein networks
6469:
6455:
6447:
6417:
6076:
6062:
6054:
5577:
5563:
5555:
5444:(covers almost all branches of proteomics)
5432:. Oxford, UK: BIOS Scientific Publishers.
3731:Moellering RE, Cravatt BF (January 2012).
2887:
2885:
188:and structural proteins in the process of
6043:Timeline of biology and organic chemistry
5503:
5386:
5300:
5182:
5133:
5084:
5027:
5017:
4941:
4900:
4851:
4841:
4768:
4758:
4717:
4668:
4512:
4463:
4414:
4404:
4355:
4345:
4268:
4219:
4119:
4070:
3982:
3756:
3707:
3697:
3578:
3537:
3344:
3282:
3240:
3192:
3069:
2793:
2752:
2668:
2576:
2535:
2525:
2484:
2474:
2390:
2290:
2252:
2242:
2193:
2109:
2012:
1938:
1814:
1757:
1708:
1659:
1649:
1608:
5539:) is being considered for deletion. See
2508:Coorssen JR, Yergey AL (December 2015).
939:, a subfield of proteomics that studies
892:that are used in expression proteomics.
674:
653:
3514:"The Future of Bioorthogonal Chemistry"
1497:
587:Mass spectrometry and protein profiling
364:differences between experiments due to
4586:
4576:
4008:Clinical Pharmacology and Therapeutics
2038:International Journal of Pharmaceutics
578:High-throughput proteomic technologies
473:More recently implemented methods use
6391:European Molecular Biology Laboratory
6038:Nobel Prize in Physiology or Medicine
5367:The Journal of Clinical Investigation
4102:Klopfleisch R, Gruber AD (May 2009).
3957:Strimbu K, Tavel JA (November 2010).
3881:10.1146/annurev-biochem-072909-100424
1154:more comprehensively. As an example,
626:Pacific Northwest National Laboratory
527:MSIA (mass spectrometric immunoassay)
7:
5424:(focused on 2D-gels, good on detail)
1915:"Government backs proteome proposal"
783:identify binary protein interactions
466:(introduced in 1967) where a single
299:dynamic complexity of the proteome.
4649:Molecular & Cellular Proteomics
4645:"Scaling Up Single-Cell Proteomics"
3659:10.1146/annurev-genet-102209-163500
3095:Current Opinion in Chemical Biology
3058:Molecular & Cellular Proteomics
1795:Current Opinion in Chemical Biology
1451:Proteomics Identifications Database
871:, is crucial towards understanding
836:, and experimental methods such as
664:laser capture microdissection (LCM)
6542:Isotope-coded affinity tags (ICAT)
3329:Quantitative Methods in Proteomics
3275:Quantitative Methods in Proteomics
2865:Broad Institute of MIT and Harvard
798:probe protein–protein interactions
650:Reverse-phased protein microarrays
14:
5543:to help reach a consensus. ›
5505:10.1161/CIRCULATIONAHA.104.482570
4493:Proteomics. Clinical Applications
1481:European Bioinformatics Institute
1219:Molecular and Cellular Proteomics
955:, proteomic technologies such as
929:enzyme linked immunosorbent assay
796:Several methods are available to
513:and then, directly ionized using
485:. These methods gave rise to the
416:enzyme-linked immunosorbent assay
6547:Metal-coded affinity tag (MeCAT)
6429:
6428:
6416:
3907:Current Opinion in Biotechnology
3782:Chemical Genomics and Proteomics
3052:Uhlen M, Ponten F (April 2005).
2941:Stål (Hemiptera: Delphacidae)".
2782:Journal of Laboratory Automation
1423:Human Protein Reference Database
1287:
1273:
1048:post-translational modifications
1042:Post-translational modifications
826:dual polarisation interferometry
804:, a powerful emerging method is
325:post-translational modifications
161:Post-translational modifications
19:For the journal Proteomics, see
6369:Chromosome conformation capture
5404:Naven T, Westermeier R (2002).
4450:(Web Server issue): W422–W426.
3963:Current Opinion in HIV and AIDS
1344:List of omics topics in biology
449:Antibody-free protein detection
295:
167:Post-translational modification
5349:(electronic, on Netlibrary?),
5213:Journal of Orthopaedic Science
5029:11858/00-001M-0000-002B-A17E-4
3749:10.1016/j.chembiol.2012.01.001
3346:11858/00-001M-0000-000F-C327-D
2735:Jayasena SD (September 1999).
2174:Molecular and Cellular Biology
2073:"The major world of microRNAs"
1838:Wittmann, H. G. (1974-01-01),
1632:Hood L, Rowen L (2013-09-13).
765:A branch of proteomics called
533:Current research methodologies
1:
6397:National Institutes of Health
5450:Proteomics Sample Preparation
4924:Anderson NL (February 2010).
3869:Annual Review of Biochemistry
3561:Vaidyanathan G (March 2012).
2670:10.1016/S0014-5793(97)01062-4
2050:10.1016/j.ijpharm.2005.04.010
2005:10.1093/bioinformatics/btn553
1913:Swinbanks D (December 1995).
1562:10.1016/S0167-7799(98)01245-1
1486:Netherlands Proteomics Centre
908:National Institutes of Health
727:Non-proteinogenic amino acids
511:reversed-phase chromatography
483:electrospray ionization (ESI)
200:mediated by serine-threonine
16:Large-scale study of proteins
6578:Data-independent acquisition
5330:. Totowa, NJ: Humana Press.
4943:10.1373/clinchem.2009.126706
4760:10.1371/journal.pbio.3001512
4622:10.1021/acs.analchem.3c04497
4406:10.1371/journal.pcbi.1003154
3975:10.1097/COH.0b013e32833ed177
3919:10.1016/j.copbio.2011.11.014
3229:Journal of Proteome Research
3134:Journal of Proteome Research
2973:Journal of Proteome Research
2955:10.1016/j.cropro.2010.07.009
2714:10.1016/j.drudis.2008.04.013
2610:Journal of Mass Spectrometry
2565:Journal of Mass Spectrometry
2371:Journal of Proteome Research
2279:Journal of Proteome Research
1852:10.1016/0076-6879(74)30050-x
1445:Protein Information Resource
1339:List of biological databases
1231:Journal of Proteome Research
1016:Protein structure prediction
925:immunohistochemical staining
779:protein–protein interactions
383:Methods of studying proteins
44:is the large-scale study of
6313:Structure-based drug design
4979:10.1016/j.jprot.2014.03.005
4661:10.1016/j.mcpro.2021.100179
4153:Expert Review of Proteomics
3823:Expert Review of Proteomics
3790:10.1007/978-1-61779-349-3_4
3393:Expert Review of Proteomics
3337:10.1007/978-1-61779-885-6_7
3284:10.1007/978-1-0716-1024-4_8
3185:10.1016/j.mgene.2015.05.004
37:samples on a sample carrier
6625:
5019:10.1016/j.cels.2016.02.015
4843:10.1186/s13059-022-02817-5
4710:10.1038/s41587-022-01389-w
4553:10.1142/9789812776136_0024
4385:PLOS Computational Biology
4121:10.1354/vp.08-VP-0212-K-FL
3580:10.1016/j.cell.2012.02.041
3530:10.1021/acscentsci.8b00251
3512:Devaraj NK (August 2018).
3107:10.1016/j.cbpa.2003.12.009
3071:10.1074/mcp.R500009-MCP200
2754:10.1093/clinchem/45.9.1628
2111:10.1016/j.cell.2006.09.026
1807:10.1016/j.cbpa.2020.04.018
1789:Slavov N (February 2021).
1750:10.1038/s41592-023-01785-3
1013:
899:
863:(GRNs, where knowledge of
590:
366:data-dependent acquisition
164:
18:
6573:Targeted proteomics / SRM
6515:Label-free quantification
6489:Protein mass spectrometry
6484:
6412:
6403:Wellcome Sanger Institute
5592:
5225:10.1007/s00776-004-0878-0
5163:Molecular Systems Biology
5114:Molecular Systems Biology
4803:10.1101/2022.03.16.484655
4741:Slavov N (January 2022).
4643:Slavov N (January 2022).
3647:Annual Review of Genetics
2559:König S (February 2021).
2071:Buckingham S (May 2003).
1304:Activity-based proteomics
1156:The Cancer Proteome Atlas
1115:environment (biophysical)
830:microscale thermophoresis
818:surface plasmon resonance
810:protein mass spectrometry
571:Macrobrachium rosenbergii
554:adult females and males.
216:active in that instance.
180:One such modification is
133:Complexity of the problem
6359:Microfluidic-based tools
6204:Human Connectome Project
6136:Human Microbiome Project
5541:templates for discussion
5293:10.1177/0300985813502819
4165:10.1586/14789450.4.2.239
4063:10.1177/0300985813502819
3835:10.1586/14789450.5.3.425
2795:10.1177/2211068215589580
2527:10.3390/proteomes3040440
2476:10.3390/proteomes8030014
1884:10.1002/elps.11501601185
1107:cellular differentiation
1035:Cryo-electron microscopy
865:protein-DNA interactions
861:gene regulatory networks
816:. Other methods include
281:cellular differentiation
235:Additional modifications
184:, which happens to many
6478:Quantitative proteomics
6344:Electrospray ionization
6216:Human Epigenome Project
5452:. Weinheim: Wiley-VCH.
5412:. Weinheim: Wiley-VCH.
4347:10.1186/1471-2105-15-95
4020:10.1067/mcp.2001.113989
3737:Chemistry & Biology
2244:10.1073/pnas.0605420103
1550:Trends in Biotechnology
1519:10.1002/elps.1150191103
1394:Yeast two-hybrid system
1160:The Cancer Genome Atlas
959:are used for improving
844:computational methods.
834:kinetic exclusion assay
685:bioorthogonal chemistry
683:Recent advancements in
614:Quantitative proteomics
559:Arabidopsis peroxisomes
30:Robotic preparation of
6530:Tandem mass tags (TMT)
6385:DNA Data Bank of Japan
6301:Human proteome project
6104:Computational genomics
5652:Biological engineering
4505:10.1002/prca.200900109
4444:Nucleic Acids Research
3959:"What are biomarkers?"
3023:10.1002/pmic.201000681
2867:. 2015. Archived from
1329:Human proteome project
1022:biomolecular structure
997:Protein identification
741:Practical applications
680:
659:
602:
38:
6364:Isotope affinity tags
6318:Expression proteomics
5737:Developmental biology
5712:Computational biology
5692:Cellular microbiology
5486:Vasan RS (May 2006).
5175:10.15252/msb.20145728
5126:10.15252/msb.20167357
5057:Nature Communications
4967:Journal of Proteomics
4797:: 2022.03.16.484655.
4261:10.1101/gr.074344.107
3944:"What is Proteomics?"
2186:10.1128/MCB.19.3.1720
1844:Methods in Enzymology
1243:Journal of Proteomics
1186:Human plasma proteome
1027:X-ray crystallography
967:Structural proteomics
879:Expression proteomics
873:systems-level biology
806:affinity purification
716:cell surface labeling
706:Recent studies using
689:Unnatural amino acids
678:
657:
600:
557:Proteome analysis of
208:mediated by tyrosine
105:History and etymology
48:. Proteins are vital
29:
6124:Human Genome Project
6109:Comparative genomics
5957:Reproductive biology
5842:Mathematical biology
5767:Evolutionary biology
5717:Conservation biology
5471:. Berlin: Springer.
5448:von Hagen J (2008).
5281:Veterinary Pathology
4698:Nature Biotechnology
4610:Analytical Chemistry
4108:Veterinary Pathology
4051:Veterinary Pathology
3699:10.3390/ijms14023921
3479:ACS Chemical Biology
3436:Nature Biotechnology
2819:Analytical Chemistry
2702:Drug Discovery Today
2416:Nature Biotechnology
2324:Nature Biotechnology
1309:Bottom-up proteomics
1180:evolutionary biology
814:tagged protein baits
731:Staudinger ligations
491:bottom-up proteomics
341:alternative splicing
313:level of translation
229:E3 ubiquitin ligases
127:Macquarie University
95:protein purification
81:Human Genome Project
21:Proteomics (journal)
6561:Acquisition methods
6552:N-terminal labeling
6334:2-D electrophoresis
6308:Call-map proteomics
6166:Structural genomics
6153:Population genomics
6114:Functional genomics
5742:Ecological genetics
5586:Branches of biology
5326:Liebler DC (2002).
5077:10.1038/ncomms10261
5069:2016NatCo...710261M
4547:. pp. 231–42.
4397:2013PLSCB...9E3154P
3518:ACS Central Science
2831:10.1021/ac00103a003
2622:2012JMSp...47..795D
2235:2006PNAS..10313004B
2229:(35): 13004–13009.
1967:www.proteome.org.au
1931:1995Natur.378..653S
1418:Human Protein Atlas
1384:Top-down proteomics
1369:Proteomic chemistry
1319:Functional genomics
869:biological networks
849:biological networks
822:protein microarrays
802:two-hybrid analysis
632:Affinity proteomics
574:protein profiling.
521:Hybrid technologies
371:targeted proteomics
315:into a protein. An
85:functional genomics
6568:Shotgun proteomics
6288:Structural biology
6099:Cognitive genomics
6033:History of biology
5967:Structural biology
5952:Relational biology
5777:Generative biology
5772:Freshwater biology
5428:Twyman RM (2004).
4930:Clinical Chemistry
4893:10.1038/nmeth.2650
4456:10.1093/nar/gkt416
4334:BMC Bioinformatics
4315:prosite.expasy.org
4311:"ExPASy - PROSITE"
4212:10.1101/gr.6427907
2939:Nilaparvata lugens
2741:Clinical Chemistry
2708:(15–16): 695–701.
2143:Clinical Chemistry
1379:Shotgun proteomics
1359:Protein production
1324:Heat stabilization
885:protein expression
746:New drug discovery
681:
660:
603:
544:Nilaparvata lugens
497:Separation methods
39:
6586:
6585:
6525:Isobaric labeling
6499:Mass spectrometry
6444:
6443:
6339:Mass spectrometer
6148:Personal genomics
6051:
6050:
5972:Synthetic biology
5852:Molecular biology
5707:Cognitive biology
5498:(19): 2335–2362.
5478:978-3-540-62753-1
5459:978-3-527-31796-7
5439:978-1-85996-273-2
5419:978-3-527-30354-0
5373:(12): 3370–3377.
5337:978-0-89603-992-6
5264:978-1-904425-53-3
4887:(11): 1046–1047.
4616:(20): 7976–8010.
4545:Biocomputing 2008
4499:(12): 1389–1396.
3799:978-1-61779-348-6
3610:(12): 2492–2500.
3491:10.1021/cb4009292
3405:10.1586/epr.12.34
3356:978-1-61779-884-9
3294:978-1-0716-1023-7
3251:10.1021/pr0499693
3146:10.1021/pr100671c
3140:(12): 6380–6391.
2985:10.1021/pr200414g
2979:(10): 4597–4612.
2383:10.1021/pr9006365
2301:10.1021/pr025556v
1999:(24): 2894–2900.
1701:10.1021/cr3003533
1601:10.1002/stem.2298
1513:(11): 1853–1861.
1439:Protein Data Bank
1411:Protein databases
1354:Phosphoproteomics
1010:Protein structure
982:mass spectrometry
957:mass spectrometry
941:secreted proteins
933:mass spectrometry
890:mass spectrometry
855:, for example in
787:protein complexes
693:functional groups
624:and coworkers at
593:Mass spectrometry
475:mass spectrometry
464:Edman degradation
458:Detection methods
393:mass spectrometry
330:phosphoproteomics
204:, or more rarely
99:mass spectrometry
35:mass spectrometry
6616:
6471:
6464:
6457:
6448:
6432:
6431:
6420:
6419:
6263:Pharmacogenomics
6258:Pharmacogenetics
6078:
6071:
6064:
6055:
5697:Chemical biology
5579:
5572:
5565:
5556:
5517:
5507:
5482:
5463:
5443:
5423:
5411:
5400:
5390:
5379:10.1172/JCI26885
5341:
5322:
5304:
5275:
5274:on 28 June 2006.
5273:
5267:. Archived from
5256:
5244:
5197:
5196:
5186:
5154:
5148:
5147:
5137:
5105:
5099:
5098:
5088:
5048:
5042:
5041:
5031:
5021:
4997:
4991:
4990:
4962:
4956:
4955:
4945:
4921:
4915:
4914:
4904:
4872:
4866:
4865:
4855:
4845:
4821:
4815:
4814:
4789:
4783:
4782:
4772:
4762:
4738:
4732:
4731:
4721:
4689:
4683:
4682:
4672:
4640:
4634:
4633:
4601:
4595:
4594:
4588:
4584:
4582:
4574:
4536:
4527:
4526:
4516:
4484:
4478:
4477:
4467:
4435:
4429:
4428:
4418:
4408:
4376:
4370:
4369:
4359:
4349:
4325:
4319:
4318:
4307:
4301:
4300:
4289:
4283:
4282:
4272:
4255:(7): 1133–1142.
4240:
4234:
4233:
4223:
4206:(9): 1362–1377.
4191:
4185:
4184:
4148:
4142:
4141:
4123:
4099:
4093:
4092:
4074:
4046:
4040:
4039:
4003:
3997:
3996:
3986:
3954:
3948:
3947:
3946:. ProteoConsult.
3940:
3931:
3930:
3902:
3893:
3892:
3864:
3855:
3854:
3818:
3812:
3811:
3777:
3771:
3770:
3760:
3728:
3722:
3721:
3711:
3701:
3692:(2): 3921–3945.
3677:
3671:
3670:
3642:
3636:
3635:
3599:
3593:
3592:
3582:
3573:(6): 1079–1080.
3558:
3552:
3551:
3541:
3509:
3503:
3502:
3474:
3468:
3467:
3448:10.1038/nbt.2356
3431:
3425:
3424:
3388:
3382:
3381:
3380:
3379:
3348:
3320:
3314:
3313:
3286:
3269:
3263:
3262:
3244:
3224:
3207:
3206:
3196:
3164:
3158:
3157:
3128:
3119:
3118:
3090:
3084:
3083:
3073:
3049:
3043:
3042:
3017:(9): 1764–1779.
3006:
2997:
2996:
2968:
2959:
2958:
2933:
2927:
2926:
2889:
2880:
2879:
2877:
2876:
2857:
2851:
2850:
2825:(7): 1153–1158.
2814:
2808:
2807:
2797:
2773:
2767:
2766:
2756:
2747:(9): 1628–1650.
2732:
2726:
2725:
2697:
2691:
2690:
2672:
2648:
2642:
2641:
2630:10.1002/jms.3038
2605:
2599:
2598:
2580:
2578:10.1002/jms.4616
2556:
2550:
2549:
2539:
2529:
2505:
2499:
2498:
2488:
2478:
2454:
2448:
2447:
2428:10.1038/nbt.1661
2411:
2405:
2404:
2394:
2362:
2356:
2355:
2319:
2313:
2312:
2294:
2273:
2267:
2266:
2256:
2246:
2214:
2208:
2207:
2197:
2180:(3): 1720–1730.
2165:
2159:
2158:
2149:(8): 1160–1169.
2138:
2132:
2131:
2113:
2089:
2083:
2082:
2080:
2079:
2068:
2062:
2061:
2033:
2027:
2026:
2016:
1984:
1978:
1977:
1975:
1974:
1959:
1953:
1952:
1942:
1940:10.1038/378653a0
1910:
1904:
1903:
1878:(7): 1090–1094.
1867:
1861:
1860:
1859:
1858:
1835:
1829:
1828:
1818:
1786:
1780:
1779:
1761:
1729:
1723:
1722:
1712:
1695:(4): 2343–2394.
1689:Chemical Reviews
1680:
1674:
1673:
1663:
1653:
1629:
1623:
1622:
1612:
1580:
1574:
1573:
1545:
1539:
1538:
1502:
1475:Research centers
1334:Immunoproteomics
1297:
1292:
1291:
1290:
1283:
1278:
1277:
1031:NMR spectroscopy
961:gene annotations
622:Richard D. Smith
112:Escherichia coli
6624:
6623:
6619:
6618:
6617:
6615:
6614:
6613:
6589:
6588:
6587:
6582:
6556:
6503:
6480:
6475:
6445:
6440:
6408:
6373:
6322:
6282:
6278:Transcriptomics
6268:Systems biology
6253:Paleopolyploidy
6189:Cheminformatics
6170:
6087:
6082:
6052:
6047:
6021:
5982:Systems biology
5947:Quantum biology
5588:
5583:
5544:
5525:
5520:
5485:
5479:
5466:
5460:
5447:
5440:
5427:
5420:
5403:
5360:
5338:
5325:
5278:
5271:
5265:
5254:
5247:
5209:
5205:
5200:
5156:
5155:
5151:
5107:
5106:
5102:
5050:
5049:
5045:
4999:
4998:
4994:
4964:
4963:
4959:
4923:
4922:
4918:
4874:
4873:
4869:
4823:
4822:
4818:
4791:
4790:
4786:
4753:(1): e3001512.
4740:
4739:
4735:
4691:
4690:
4686:
4642:
4641:
4637:
4603:
4602:
4598:
4585:
4575:
4563:
4538:
4537:
4530:
4486:
4485:
4481:
4437:
4436:
4432:
4391:(7): e1003154.
4378:
4377:
4373:
4327:
4326:
4322:
4309:
4308:
4304:
4297:www.uniprot.org
4291:
4290:
4286:
4249:Genome Research
4242:
4241:
4237:
4200:Genome Research
4193:
4192:
4188:
4150:
4149:
4145:
4101:
4100:
4096:
4048:
4047:
4043:
4005:
4004:
4000:
3956:
3955:
3951:
3942:
3941:
3934:
3904:
3903:
3896:
3866:
3865:
3858:
3820:
3819:
3815:
3800:
3779:
3778:
3774:
3730:
3729:
3725:
3679:
3678:
3674:
3644:
3643:
3639:
3604:Electrophoresis
3601:
3600:
3596:
3560:
3559:
3555:
3511:
3510:
3506:
3476:
3475:
3471:
3442:(10): 984–990.
3433:
3432:
3428:
3390:
3389:
3385:
3377:
3375:
3357:
3322:
3321:
3317:
3295:
3271:
3270:
3266:
3242:10.1.1.603.4384
3226:
3225:
3210:
3166:
3165:
3161:
3130:
3129:
3122:
3092:
3091:
3087:
3051:
3050:
3046:
3008:
3007:
3000:
2970:
2969:
2962:
2943:Crop Protection
2935:
2934:
2930:
2891:
2890:
2883:
2874:
2872:
2859:
2858:
2854:
2816:
2815:
2811:
2775:
2774:
2770:
2734:
2733:
2729:
2699:
2698:
2694:
2650:
2649:
2645:
2607:
2606:
2602:
2558:
2557:
2553:
2507:
2506:
2502:
2456:
2455:
2451:
2413:
2412:
2408:
2364:
2363:
2359:
2321:
2320:
2316:
2275:
2274:
2270:
2216:
2215:
2211:
2167:
2166:
2162:
2140:
2139:
2135:
2091:
2090:
2086:
2077:
2075:
2070:
2069:
2065:
2035:
2034:
2030:
1986:
1985:
1981:
1972:
1970:
1961:
1960:
1956:
1912:
1911:
1907:
1872:Electrophoresis
1869:
1868:
1864:
1856:
1854:
1837:
1836:
1832:
1788:
1787:
1783:
1731:
1730:
1726:
1682:
1681:
1677:
1638:Genome Medicine
1631:
1630:
1626:
1582:
1581:
1577:
1547:
1546:
1542:
1507:Electrophoresis
1504:
1503:
1499:
1495:
1477:
1472:
1413:
1408:
1389:Systems biology
1295:Medicine portal
1293:
1288:
1286:
1279:
1272:
1269:
1201:
1188:
1136:transcriptomics
1119:Transcriptional
1098:
1096:Systems biology
1089:
1087:Emerging trends
1056:
1044:
1018:
1012:
999:
978:
969:
949:
904:
898:
881:
853:systems biology
775:
767:chemoproteomics
748:
743:
673:
652:
643:
634:
595:
589:
580:
535:
523:
507:two-dimensional
503:one-dimensional
499:
460:
451:
401:
385:
354:Reproducibility
334:glycoproteomics
305:
273:
241:phosphorylation
239:In addition to
237:
222:
182:phosphorylation
178:
176:Phosphorylation
169:
163:
143:transcriptomics
135:
107:
24:
17:
12:
11:
5:
6622:
6620:
6612:
6611:
6606:
6601:
6591:
6590:
6584:
6583:
6581:
6580:
6575:
6570:
6564:
6562:
6558:
6557:
6555:
6554:
6549:
6544:
6539:
6538:
6537:
6532:
6522:
6517:
6511:
6509:
6508:Quantification
6505:
6504:
6502:
6501:
6496:
6491:
6485:
6482:
6481:
6476:
6474:
6473:
6466:
6459:
6451:
6442:
6441:
6439:
6438:
6426:
6413:
6410:
6409:
6407:
6406:
6400:
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6388:
6381:
6379:
6375:
6374:
6372:
6371:
6366:
6361:
6356:
6351:
6346:
6341:
6336:
6330:
6328:
6327:Research tools
6324:
6323:
6321:
6320:
6315:
6310:
6305:
6304:
6303:
6292:
6290:
6284:
6283:
6281:
6280:
6275:
6273:Toxicogenomics
6270:
6265:
6260:
6255:
6250:
6245:
6240:
6235:
6230:
6225:
6220:
6219:
6218:
6208:
6207:
6206:
6196:
6191:
6186:
6180:
6178:
6176:Bioinformatics
6172:
6171:
6169:
6168:
6163:
6155:
6150:
6145:
6140:
6139:
6138:
6128:
6127:
6126:
6119:Genome project
6116:
6111:
6106:
6101:
6095:
6093:
6089:
6088:
6083:
6081:
6080:
6073:
6066:
6058:
6049:
6048:
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6045:
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6019:
6014:
6009:
6004:
5999:
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5979:
5974:
5969:
5964:
5959:
5954:
5949:
5944:
5939:
5934:
5929:
5924:
5919:
5914:
5909:
5904:
5899:
5894:
5889:
5884:
5879:
5874:
5869:
5864:
5859:
5854:
5849:
5844:
5839:
5837:Marine biology
5834:
5829:
5824:
5819:
5814:
5809:
5804:
5799:
5794:
5789:
5784:
5779:
5774:
5769:
5764:
5759:
5754:
5749:
5744:
5739:
5734:
5729:
5724:
5719:
5714:
5709:
5704:
5699:
5694:
5689:
5684:
5679:
5674:
5669:
5664:
5659:
5654:
5649:
5647:Bioinformatics
5644:
5639:
5634:
5629:
5624:
5619:
5614:
5609:
5604:
5599:
5593:
5590:
5589:
5584:
5582:
5581:
5574:
5567:
5559:
5553:
5552:
5528:
5524:
5523:External links
5521:
5519:
5518:
5483:
5477:
5464:
5458:
5445:
5438:
5425:
5418:
5401:
5358:
5336:
5323:
5276:
5263:
5245:
5219:(2): 160–166.
5206:
5204:
5201:
5199:
5198:
5149:
5100:
5043:
5012:(3): 185–195.
4992:
4957:
4936:(2): 177–185.
4916:
4881:Nature Methods
4867:
4830:Genome Biology
4816:
4784:
4733:
4684:
4635:
4596:
4587:|journal=
4561:
4528:
4479:
4430:
4371:
4320:
4302:
4284:
4235:
4186:
4159:(2): 239–248.
4143:
4114:(3): 416–422.
4094:
4057:(2): 351–362.
4041:
3998:
3969:(6): 463–466.
3949:
3932:
3913:(4): 591–597.
3894:
3875:(1): 379–405.
3856:
3829:(3): 425–433.
3813:
3798:
3772:
3723:
3672:
3637:
3594:
3553:
3524:(8): 952–959.
3504:
3469:
3426:
3399:(4): 401–414.
3383:
3355:
3315:
3293:
3264:
3235:(2): 179–196.
3208:
3159:
3120:
3085:
3064:(4): 384–393.
3044:
2998:
2960:
2949:(11): 1280–5.
2928:
2901:(3): 377–396.
2881:
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2809:
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2768:
2727:
2692:
2663:(3): 521–526.
2643:
2616:(6): 795–809.
2600:
2551:
2520:(4): 440–453.
2500:
2449:
2422:(7): 710–721.
2406:
2377:(2): 761–776.
2357:
2330:(3): 242–247.
2314:
2292:10.1.1.460.237
2268:
2209:
2160:
2133:
2104:(3): 635–648.
2084:
2063:
2028:
1993:Bioinformatics
1979:
1954:
1905:
1862:
1830:
1781:
1744:(3): 375–386.
1738:Nature Methods
1724:
1675:
1624:
1595:(3): 601–613.
1575:
1556:(3): 121–127.
1540:
1496:
1494:
1491:
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1483:
1476:
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1471:
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1391:
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1381:
1376:
1371:
1366:
1364:Proteogenomics
1361:
1356:
1351:
1346:
1341:
1336:
1331:
1326:
1321:
1316:
1311:
1306:
1300:
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1298:
1284:
1281:Biology portal
1268:
1265:
1264:
1263:
1251:
1239:
1227:
1200:
1197:
1187:
1184:
1164:cancer biology
1111:carcinogenesis
1097:
1094:
1088:
1085:
1061:fetal proteins
1055:
1052:
1043:
1040:
1033:. As of 2017,
1014:Main article:
1011:
1008:
998:
995:
987:bioinformatics
977:
974:
968:
965:
953:proteogenomics
948:
947:Proteogenomics
945:
900:Main article:
897:
894:
880:
877:
857:cell signaling
774:
771:
747:
744:
742:
739:
672:
669:
651:
648:
642:
639:
633:
630:
591:Main article:
588:
585:
579:
576:
534:
531:
522:
519:
498:
495:
459:
456:
450:
447:
435:phosphorylated
400:
397:
384:
381:
351:
350:
347:
344:
337:
320:
304:
301:
289:carcinogenesis
272:
269:
245:ubiquitination
236:
233:
221:
220:Ubiquitination
218:
190:cell signaling
177:
174:
165:Main article:
162:
159:
134:
131:
106:
103:
50:macromolecules
15:
13:
10:
9:
6:
4:
3:
2:
6621:
6610:
6607:
6605:
6602:
6600:
6597:
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6574:
6571:
6569:
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6543:
6540:
6536:
6533:
6531:
6528:
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6523:
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6510:
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6500:
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6483:
6479:
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6465:
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6436:
6427:
6425:
6424:
6415:
6414:
6411:
6404:
6401:
6398:
6395:
6392:
6389:
6386:
6383:
6382:
6380:
6378:Organizations
6376:
6370:
6367:
6365:
6362:
6360:
6357:
6355:
6352:
6350:
6347:
6345:
6342:
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6319:
6316:
6314:
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6274:
6271:
6269:
6266:
6264:
6261:
6259:
6256:
6254:
6251:
6249:
6248:Nutrigenomics
6246:
6244:
6241:
6239:
6236:
6234:
6231:
6229:
6226:
6224:
6221:
6217:
6214:
6213:
6212:
6209:
6205:
6202:
6201:
6200:
6197:
6195:
6194:Chemogenomics
6192:
6190:
6187:
6185:
6182:
6181:
6179:
6177:
6173:
6167:
6164:
6162:
6160:
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6151:
6149:
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6137:
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6112:
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5943:
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5930:
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5918:
5917:Phylogenetics
5915:
5913:
5910:
5908:
5905:
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5900:
5898:
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5890:
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5838:
5835:
5833:
5830:
5828:
5825:
5823:
5820:
5818:
5815:
5813:
5812:Human biology
5810:
5808:
5805:
5803:
5800:
5798:
5795:
5793:
5790:
5788:
5785:
5783:
5780:
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5770:
5768:
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5743:
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5728:
5725:
5723:
5720:
5718:
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5713:
5710:
5708:
5705:
5703:
5702:Chronobiology
5700:
5698:
5695:
5693:
5690:
5688:
5685:
5683:
5680:
5678:
5677:Biotechnology
5675:
5673:
5672:Biostatistics
5670:
5668:
5665:
5663:
5660:
5658:
5655:
5653:
5650:
5648:
5645:
5643:
5640:
5638:
5635:
5633:
5630:
5628:
5625:
5623:
5620:
5618:
5615:
5613:
5610:
5608:
5605:
5603:
5600:
5598:
5595:
5594:
5591:
5587:
5580:
5575:
5573:
5568:
5566:
5561:
5560:
5557:
5551:
5547:
5542:
5538:
5537:
5532:
5527:
5526:
5522:
5515:
5511:
5506:
5501:
5497:
5493:
5489:
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5470:
5465:
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5426:
5421:
5415:
5410:
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5402:
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5389:
5384:
5380:
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5368:
5364:
5359:
5356:
5355:0-89603-991-9
5352:
5348:
5347:0-585-41879-9
5344:
5339:
5333:
5329:
5324:
5320:
5316:
5312:
5308:
5303:
5298:
5294:
5290:
5287:(2): 351–62.
5286:
5282:
5277:
5270:
5266:
5260:
5253:
5252:
5246:
5242:
5238:
5234:
5230:
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4920:
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4882:
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4868:
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4703:
4699:
4695:
4688:
4685:
4680:
4676:
4671:
4666:
4662:
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4655:(1): 100179.
4654:
4650:
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4631:
4627:
4623:
4619:
4615:
4611:
4607:
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3508:
3505:
3500:
3496:
3492:
3488:
3484:
3480:
3473:
3470:
3465:
3461:
3457:
3453:
3449:
3445:
3441:
3437:
3430:
3427:
3422:
3418:
3414:
3410:
3406:
3402:
3398:
3394:
3387:
3384:
3374:
3370:
3366:
3362:
3358:
3352:
3347:
3342:
3338:
3334:
3330:
3326:
3319:
3316:
3312:
3308:
3304:
3300:
3296:
3290:
3285:
3280:
3276:
3268:
3265:
3260:
3256:
3252:
3248:
3243:
3238:
3234:
3230:
3223:
3221:
3219:
3217:
3215:
3213:
3209:
3204:
3200:
3195:
3190:
3186:
3182:
3178:
3174:
3170:
3163:
3160:
3155:
3151:
3147:
3143:
3139:
3135:
3127:
3125:
3121:
3116:
3112:
3108:
3104:
3100:
3096:
3089:
3086:
3081:
3077:
3072:
3067:
3063:
3059:
3055:
3048:
3045:
3040:
3036:
3032:
3028:
3024:
3020:
3016:
3012:
3005:
3003:
2999:
2994:
2990:
2986:
2982:
2978:
2974:
2967:
2965:
2961:
2956:
2952:
2948:
2944:
2940:
2932:
2929:
2924:
2920:
2916:
2912:
2908:
2904:
2900:
2896:
2888:
2886:
2882:
2871:on 2015-07-15
2870:
2866:
2862:
2856:
2853:
2848:
2844:
2840:
2836:
2832:
2828:
2824:
2820:
2813:
2810:
2805:
2801:
2796:
2791:
2787:
2783:
2779:
2772:
2769:
2764:
2760:
2755:
2750:
2746:
2742:
2738:
2731:
2728:
2723:
2719:
2715:
2711:
2707:
2703:
2696:
2693:
2688:
2684:
2680:
2676:
2671:
2666:
2662:
2658:
2654:
2647:
2644:
2639:
2635:
2631:
2627:
2623:
2619:
2615:
2611:
2604:
2601:
2596:
2592:
2588:
2584:
2579:
2574:
2570:
2566:
2562:
2555:
2552:
2547:
2543:
2538:
2533:
2528:
2523:
2519:
2515:
2511:
2504:
2501:
2496:
2492:
2487:
2482:
2477:
2472:
2468:
2464:
2460:
2453:
2450:
2445:
2441:
2437:
2433:
2429:
2425:
2421:
2417:
2410:
2407:
2402:
2398:
2393:
2388:
2384:
2380:
2376:
2372:
2368:
2361:
2358:
2353:
2349:
2345:
2341:
2337:
2336:10.1038/85686
2333:
2329:
2325:
2318:
2315:
2310:
2306:
2302:
2298:
2293:
2288:
2284:
2280:
2272:
2269:
2264:
2260:
2255:
2250:
2245:
2240:
2236:
2232:
2228:
2224:
2220:
2213:
2210:
2205:
2201:
2196:
2191:
2187:
2183:
2179:
2175:
2171:
2164:
2161:
2156:
2152:
2148:
2144:
2137:
2134:
2129:
2125:
2121:
2117:
2112:
2107:
2103:
2099:
2095:
2088:
2085:
2074:
2067:
2064:
2059:
2055:
2051:
2047:
2044:(1–2): 1–18.
2043:
2039:
2032:
2029:
2024:
2020:
2015:
2010:
2006:
2002:
1998:
1994:
1990:
1983:
1980:
1968:
1964:
1958:
1955:
1950:
1946:
1941:
1936:
1932:
1928:
1925:(6558): 653.
1924:
1920:
1916:
1909:
1906:
1901:
1897:
1893:
1889:
1885:
1881:
1877:
1873:
1866:
1863:
1853:
1849:
1845:
1841:
1834:
1831:
1826:
1822:
1817:
1812:
1808:
1804:
1800:
1796:
1792:
1785:
1782:
1777:
1773:
1769:
1765:
1760:
1755:
1751:
1747:
1743:
1739:
1735:
1728:
1725:
1720:
1716:
1711:
1706:
1702:
1698:
1694:
1690:
1686:
1679:
1676:
1671:
1667:
1662:
1657:
1652:
1651:10.1186/gm483
1647:
1643:
1639:
1635:
1628:
1625:
1620:
1616:
1611:
1606:
1602:
1598:
1594:
1590:
1586:
1579:
1576:
1571:
1567:
1563:
1559:
1555:
1551:
1544:
1541:
1536:
1532:
1528:
1524:
1520:
1516:
1512:
1508:
1501:
1498:
1492:
1487:
1484:
1482:
1479:
1478:
1474:
1469:
1466:
1464:
1461:
1458:
1455:
1452:
1449:
1446:
1443:
1440:
1437:
1435:
1432:
1429:
1426:
1424:
1421:
1419:
1416:
1415:
1410:
1405:
1402:
1400:
1397:
1395:
1392:
1390:
1387:
1385:
1382:
1380:
1377:
1375:
1372:
1370:
1367:
1365:
1362:
1360:
1357:
1355:
1352:
1350:
1347:
1345:
1342:
1340:
1337:
1335:
1332:
1330:
1327:
1325:
1322:
1320:
1317:
1315:
1312:
1310:
1307:
1305:
1302:
1301:
1296:
1285:
1282:
1276:
1271:
1266:
1261:
1257:
1256:
1252:
1249:
1245:
1244:
1240:
1237:
1233:
1232:
1228:
1225:
1221:
1220:
1216:
1215:
1214:
1212:
1208:
1207:
1198:
1196:
1192:
1185:
1183:
1181:
1177:
1173:
1169:
1168:developmental
1165:
1161:
1157:
1153:
1149:
1145:
1141:
1137:
1133:
1129:
1124:
1123:translational
1120:
1116:
1112:
1108:
1104:
1095:
1093:
1086:
1084:
1081:
1076:
1074:
1070:
1066:
1062:
1053:
1051:
1049:
1041:
1039:
1036:
1032:
1028:
1023:
1017:
1009:
1007:
1005:
996:
994:
992:
988:
983:
975:
973:
966:
964:
962:
958:
954:
946:
944:
942:
938:
934:
930:
926:
922:
916:
912:
909:
903:
895:
893:
891:
886:
878:
876:
874:
870:
866:
862:
859:cascades and
858:
854:
850:
845:
843:
839:
838:phage display
835:
831:
827:
823:
819:
815:
811:
807:
803:
799:
794:
792:
788:
784:
780:
772:
770:
768:
763:
760:
757:
753:
745:
740:
738:
734:
732:
728:
724:
719:
717:
713:
709:
704:
702:
701:perturbations
696:
694:
690:
686:
677:
670:
668:
665:
656:
649:
647:
641:Protein chips
640:
638:
631:
629:
627:
623:
618:
615:
611:
607:
599:
594:
586:
584:
577:
575:
573:
572:
566:
562:
560:
555:
553:
549:
545:
539:
532:
530:
528:
520:
518:
516:
512:
508:
504:
496:
494:
492:
488:
484:
480:
476:
471:
469:
465:
457:
455:
448:
446:
442:
438:
436:
432:
427:
425:
421:
417:
413:
409:
405:
398:
396:
394:
390:
382:
380:
378:
374:
372:
367:
363:
359:
355:
348:
345:
342:
338:
335:
331:
327:
326:
321:
318:
314:
310:
309:
308:
302:
300:
297:
292:
290:
286:
282:
278:
270:
268:
266:
265:nitrosylation
262:
258:
257:glycosylation
254:
250:
246:
242:
234:
232:
230:
226:
219:
217:
213:
211:
207:
203:
199:
195:
191:
187:
183:
175:
173:
168:
160:
158:
155:
150:
148:
144:
140:
132:
130:
128:
124:
120:
116:
114:
113:
104:
102:
100:
96:
92:
88:
86:
82:
77:
74:
69:
67:
63:
59:
55:
54:muscle tissue
51:
47:
43:
36:
33:
28:
22:
6493:
6433:
6421:
6295:
6243:Microbiomics
6238:Metabolomics
6199:Connectomics
6158:
6131:Metagenomics
5962:Sociobiology
5942:Protistology
5936:
5907:Photobiology
5902:Pharmacology
5892:Parasitology
5887:Paleontology
5867:Neuroscience
5847:Microbiology
5757:Epidemiology
5727:Cytogenetics
5687:Cell biology
5667:Biosemiotics
5657:Biomechanics
5637:Biogeography
5632:Biochemistry
5627:Bacteriology
5622:Astrobiology
5534:
5495:
5491:
5468:
5449:
5429:
5407:
5370:
5366:
5327:
5284:
5280:
5269:the original
5250:
5216:
5212:
5203:Bibliography
5166:
5162:
5152:
5117:
5113:
5103:
5060:
5056:
5046:
5009:
5006:Cell Systems
5005:
4995:
4970:
4966:
4960:
4933:
4929:
4919:
4884:
4880:
4870:
4833:
4829:
4819:
4794:
4787:
4750:
4747:PLOS Biology
4746:
4736:
4704:(1): 50–59.
4701:
4697:
4687:
4652:
4648:
4638:
4613:
4609:
4599:
4544:
4496:
4492:
4482:
4447:
4443:
4433:
4388:
4384:
4374:
4337:
4333:
4323:
4314:
4305:
4296:
4287:
4252:
4248:
4238:
4203:
4199:
4189:
4156:
4152:
4146:
4111:
4107:
4097:
4054:
4050:
4044:
4014:(3): 89–95.
4011:
4007:
4001:
3966:
3962:
3952:
3910:
3906:
3872:
3868:
3826:
3822:
3816:
3781:
3775:
3743:(1): 11–22.
3740:
3736:
3726:
3689:
3685:
3675:
3650:
3646:
3640:
3607:
3603:
3597:
3570:
3566:
3556:
3521:
3517:
3507:
3485:(1): 16–20.
3482:
3478:
3472:
3439:
3435:
3429:
3396:
3392:
3386:
3376:, retrieved
3328:
3318:
3274:
3267:
3232:
3228:
3176:
3172:
3162:
3137:
3133:
3101:(1): 33–41.
3098:
3094:
3088:
3061:
3057:
3047:
3014:
3010:
2976:
2972:
2946:
2942:
2938:
2931:
2898:
2894:
2873:. Retrieved
2869:the original
2864:
2855:
2822:
2818:
2812:
2785:
2781:
2771:
2744:
2740:
2730:
2705:
2701:
2695:
2660:
2657:FEBS Letters
2656:
2646:
2613:
2609:
2603:
2571:(2): e4616.
2568:
2564:
2554:
2517:
2513:
2503:
2466:
2462:
2452:
2419:
2415:
2409:
2374:
2370:
2360:
2327:
2323:
2317:
2285:(1): 43–50.
2282:
2278:
2271:
2226:
2222:
2212:
2177:
2173:
2163:
2146:
2142:
2136:
2101:
2097:
2087:
2076:. Retrieved
2066:
2041:
2037:
2031:
1996:
1992:
1982:
1971:. Retrieved
1966:
1957:
1922:
1918:
1908:
1875:
1871:
1865:
1855:, retrieved
1843:
1833:
1798:
1794:
1784:
1741:
1737:
1727:
1692:
1688:
1678:
1641:
1637:
1627:
1592:
1588:
1578:
1553:
1549:
1543:
1510:
1506:
1500:
1434:PeptideAtlas
1253:
1241:
1229:
1217:
1210:
1204:
1202:
1193:
1189:
1155:
1146:, and other
1144:metabolomics
1128:holistically
1099:
1090:
1077:
1057:
1045:
1019:
1000:
979:
970:
950:
921:western blot
917:
913:
905:
882:
846:
841:
808:followed by
795:
791:interactomes
776:
764:
761:
749:
735:
723:azide groups
720:
705:
697:
691:and various
682:
661:
644:
635:
619:
612:
608:
604:
581:
569:
567:
563:
558:
556:
551:
547:
543:
540:
536:
524:
500:
472:
461:
452:
443:
439:
428:
420:western blot
412:cell biology
408:biochemistry
402:
386:
377:Data quality
376:
375:
353:
352:
323:
312:
306:
293:
274:
238:
223:
214:
179:
170:
151:
136:
123:Marc Wilkins
118:
117:
110:
108:
90:
89:
78:
70:
41:
40:
6211:Epigenomics
6143:Pangenomics
6012:Xenobiology
6007:Virophysics
5977:Systematics
5932:Primatology
5877:Ornithology
5817:Ichthyology
5802:Herpetology
5797:Gerontology
5762:Epigenetics
5722:Cryobiology
5612:Agrostology
5602:Aerobiology
5597:Abiogenesis
5529:‹ The
5492:Circulation
5302:2434/226049
5120:(12): 901.
4072:2434/226049
1457:Proteopedia
1374:Secretomics
1140:epigenomics
1065:whole blood
937:Secretomics
931:(ELISA) or
277:development
253:acetylation
249:methylation
6599:Proteomics
6593:Categories
6494:Proteomics
6296:Proteomics
6233:Lipidomics
6228:Immunomics
5997:Toxicology
5992:Teratology
5937:Proteomics
5922:Physiology
5862:Neontology
5827:Lipidology
5822:Immunology
5792:Geobiology
5752:Embryology
5732:Dendrology
5662:Biophysics
5642:Biogeology
5546:Proteomics
5169:(1): 786.
4836:(1): 261.
4340:(95): 95.
3378:2023-04-14
3011:Proteomics
2895:Proteomics
2875:2015-07-15
2078:2009-01-14
1973:2017-02-06
1857:2024-08-28
1589:Stem Cells
1493:References
1463:Swiss-Prot
1349:PEGylation
1255:Proteomics
1211:proteomics
1152:phenotypes
1103:cell cycle
1073:biomarkers
896:Biomarkers
583:proteins.
441:aptamers.
404:Antibodies
389:antibodies
362:stochastic
285:cell cycle
91:Proteomics
62:antibodies
42:Proteomics
6223:Glycomics
5912:Phycology
5897:Pathology
5882:Osteology
5872:Nutrition
5832:Mammalogy
5807:Histology
5063:: 10261.
4973:: 24–30.
4811:247599981
4630:0003-2700
4589:ignored (
4579:cite book
4293:"UniProt"
3311:233740602
3237:CiteSeerX
3179:: 55–67.
3173:Meta Gene
2595:221827335
2514:Proteomes
2469:(3): 14.
2463:Proteomes
2287:CiteSeerX
1797:. Omics.
1776:251018292
1644:(9): 79.
1404:Glycomics
1174:biology,
1172:stem cell
1117:, etc.).
1080:biomarker
902:Biomarker
842:in silico
712:aldehydes
552:N. lugens
548:N. lugens
296:biomarker
261:oxidation
225:Ubiquitin
198:threonine
147:expressed
6604:Genomics
6435:Category
6161:genomics
6085:Genomics
6026:See also
6002:Virology
5987:Taxonomy
5927:Pomology
5857:Mycology
5787:Genomics
5782:Genetics
5607:Agronomy
5531:template
5514:16702488
5397:16322782
5319:25693263
5311:24045891
5241:45193214
5233:15815863
5193:25652787
5144:28007936
5095:26732734
5038:27135364
4987:24642211
4952:19884488
4911:24037243
4862:36527135
4779:34986167
4728:35835881
4679:34808355
4571:18229689
4523:20186258
4474:23703210
4425:23874192
4366:24694083
4279:18426904
4230:17690205
4181:26169223
4173:17425459
4138:11583190
4130:19176491
4089:25693263
4081:24045891
4028:11240971
3993:20978388
3927:22169889
3889:22439968
3851:11772983
3843:18532910
3808:21964781
3767:22284350
3718:23434671
3667:20649414
3653:: 1–24.
3632:24979515
3624:10939463
3589:22424218
3548:30159392
3499:24432752
3456:23000932
3421:19727645
3413:22967077
3373:33009117
3365:22665296
3303:33950486
3259:15113093
3203:26106581
3154:20932060
3115:15036154
3080:15695805
3039:20337179
3031:21472859
2993:21800909
2923:22432028
2915:11680884
2847:15134097
2804:26077162
2763:10471678
2722:18621567
2638:22707172
2587:32955142
2546:28248279
2495:32640657
2444:12367142
2436:20622845
2401:19921851
2352:16796135
2344:11231557
2309:12643542
2263:16916930
2204:10022859
2155:12142368
2120:17081983
2058:15979831
2023:18974169
1825:32599342
1768:36864200
1759:10130941
1719:23438204
1670:24040834
1619:26782178
1570:10189717
1535:28933890
1314:Cytomics
1267:See also
1248:Elsevier
1206:proteins
1199:Journals
1176:medicine
1132:genomics
756:proteome
489:and the
487:top-down
431:antibody
424:SDS-PAGE
206:tyrosine
139:genomics
119:Proteome
73:proteome
66:hormones
46:proteins
6184:Biochip
6017:Zoology
5747:Ecology
5617:Anatomy
5533:below (
5388:1297260
5184:4358658
5135:5199119
5086:4729823
5065:Bibcode
4902:4076789
4853:9756690
4795:bioRxiv
4770:8765665
4719:9839897
4670:8683604
4514:2825712
4465:3692090
4416:3715417
4393:Bibcode
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