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Current Chemical Biology Tools for Studying Protein Phosphorylation and Dephosphorylation
Author(s) -
H. S. Lu Candy,
Liu Kai,
Tan Lay Pheng,
Yao Shao Q.
Publication year - 2012
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201103206
Subject(s) - dephosphorylation , phosphorylation , protein phosphorylation , biology , proteome , kinase , drug discovery , phosphoproteomics , proteomics , phosphatase , biochemistry , computational biology , microbiology and biotechnology , protein kinase a , gene
Amongst different posttranslational events involved in cellular‐signaling pathways, phosphorylation and dephosphorylation of proteins are the most prevalent. Aberrant regulations in the cellular phosphoproteome network are implicated in most major human diseases. Consequently, kinases and phosphatases are two of the most important groups of drug targets in medicinal research today. A major challenge in the understanding of protein phosphorylation and dephosphorylation is the sheer complexity of the phosphoproteome network and the lack of tools capable of studying protein phosphorylation and dephosphorylation as they occur in cells. We highlight herein various chemical biology tools that have emerged in the last decade for such studies. First, we discuss the use of small‐molecule mimics of phosphoamino acids and their use in elucidating the function of protein phosphorylation and dephosphorylation. We also introduce recent advances in the field of activity‐based protein profiling (ABPP) for proteome‐wide detection of protein phosphorylation and dephosphorylation. We next discuss the key concepts in the design of peptide‐ and protein‐based biosensors capable of real‐time reporting of phosphorylation/dephosphorylation events. Finally, we highlight the application of peptide and small‐molecule microarrays (SMMs), and their applications in high‐throughput screening and discovery of new compounds related to phosphorylation/dephosphorylation.