
Mass Spectrometry‐Based Identification of Protein Kinase Substrates Utilizing Engineered Kinases and Thiophosphate Labeling
Author(s) -
Chi Yong,
Clurman Bruce E.
Publication year - 2010
Publication title -
current protocols in chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 14
ISSN - 2160-4762
DOI - 10.1002/9780470559277.ch100151
Subject(s) - thiophosphate , kinase , biochemistry , chemistry , enzyme , mass spectrometry , protein kinase a , microbiology and biotechnology , biology , chromatography , organic chemistry
Protein kinases constitute a large enzyme family with key roles in cellular signal transduction. One way to elucidate the functions of protein kinases is to systematically identify their downstream targets. Presented here is a simple and effective method to identify direct protein kinase substrates in native cell lysates. First, the activity of the kinase of interest is isolated by engineering the normal kinase to utilize bulky ATP analogs that cannot be used by normal cellular kinases. This allows specific labeling of substrates with thiophosphate tags by performing kinase reactions in cell lysates that also include bulky ATP‐γ‐S analogs. After digesting the proteins in the reaction mixture, thiophosphopeptides are isolated using a single‐step capture‐and‐release protocol and identified by mass spectrometry. This technique is easy to use and generally applicable. Curr. Protoc. Chem. Biol . 2:219‐234 © 2010 by John Wiley & Sons, Inc.