Quantitative Dynamics of Phosphoproteome: The Devil Is in the Details
Author(s) -
Mogjiborahman Salek,
Oreste Acuto
Publication year - 2012
Publication title -
analytical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.117
H-Index - 332
eISSN - 1520-6882
pISSN - 0003-2700
DOI - 10.1021/ac301833k
Subject(s) - chemistry , phosphorylation , computational biology , dynamics (music) , proteomics , quantitative proteomics , proteome , grasp , posttranslational modification , protein phosphorylation , mechanism (biology) , nanotechnology , computer science , biochemistry , protein kinase a , biology , acoustics , philosophy , epistemology , programming language , physics , enzyme , materials science , gene
Recent advances in peptide-based (bottom-up) quantitative proteomics and bioinformatics have opened unprecedented opportunities for extensive investigation of cellular proteomes and their dynamics. Here we discuss two approaches currently used to investigate the global dynamics of phosphorylation based on the isolation of phosphorylated proteins or peptides. We evaluate the accuracy of these methodologies to grasp the global dynamics of phosphorylation, and we raise awareness on ambiguities inherent to these analyses. We conclude that further development of targeted approaches should prevent inaccurate conclusions about the nature of biological regulations and in particular kinase-substrate networks.
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