Literature DB >> 26933738

Chemical Methods for Encoding and Decoding of Posttranslational Modifications.

Kelly N Chuh1, Anna R Batt1, Matthew R Pratt2.   

Abstract

A large array of posttranslational modifications can dramatically change the properties of proteins and influence different aspects of their biological function such as enzymatic activity, binding interactions, and proteostasis. Despite the significant knowledge that has been gained about the function of posttranslational modifications using traditional biological techniques, the analysis of the site-specific effects of a particular modificatioical">n, the ideical">ntificatioical">n of the full complemeical">nt of modified proteiical">ns iical">n the proteome, and the detectioical">n of new types of modificatioical">ns remaiical">ns challeical">ngiical">ng. Over the years, chemical methods have coical">ntributed significantly iical">n both of these areas of research. This review highlights several posttranslational modifications where chemistry-based approaches have made significant contributions to our ability to both prepare homogeneously modified proteins and identify and characterize particular modifications in complex biological settings. As the number and chemical diversity of documented posttranslational modifications continues to rise, we believe that chemical strategies will be essential to advance the field in years to come.
Copyright © 2016 Elsevier Ltd. All rights reserved.

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Year:  2016        PMID: 26933738      PMCID: PMC4779183          DOI: 10.1016/j.chembiol.2015.11.006

Source DB:  PubMed          Journal:  Cell Chem Biol        ISSN: 2451-9448            Impact factor:   8.116


  222 in total

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  33 in total

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8.  Metabolic Labeling for the Visualization and Identification of Potentially O-GlcNAc-Modified Proteins.

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10.  The Metabolic Chemical Reporter 6-Azido-6-deoxy-glucose Further Reveals the Substrate Promiscuity of O-GlcNAc Transferase and Catalyzes the Discovery of Intracellular Protein Modification by O-Glucose.

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