MassIVE MSV000084499

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Profiling of kinase-dependent signaling networks by kinobead/LC-MS analyses of phosphorylation and protein complexes

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Description

Kinase-catalyzed protein phosphorylation is fundamental to eukaryotic signal transduction, regulating most cellular processes. Kinases are also frequently dysregulated in cancer, inflammatory diseases and degenerative disorders, and because they can be inhibited with ATP-competitive molecules they now serve as important drug targets. Accordingly, analytical approaches that determine kinase activation states are critically important to understand kinase-dependent signal transduction, and to identify novel drug targets and predictive biomarkers. Multiplexed inhibitor beads (MIBs or kinobeads) efficiently enrich kinases from cell lysates for LC-MS analysis. When combined with phosphopeptide enrichment, kinobead/LC-MS can also quantify the phosphorylation state of kinases, allowing determination of their activation state. However, an efficient kinobead/LC-MS kinase phospho-profiling protocol that allows routine analyses of cell lines and tissues has not yet been developed. Here, we present a facile workflow that quantifies the global phosphorylation state of kinases with unprecedented sensitivity. We also found that our kinobead/LC-MS protocol can measure changes in kinase complex composition and show how these changes can indicate kinase activity. We demonstrate the utility of our approach in specifying kinase signaling pathways that control the acute steroidogenic response in Leydig cells; this analysis establishes the first comprehensive framework for the post-translational control of steroid biosynthesis. [doi:10.25345/C51D4G] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Mass spectrometry, chemoproteomics, kinobeads, protein kinase, steroidogenesis

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Principal Investigators:
(in alphabetical order) 		Shao-En Ong, University of Washington, United States
Submitting User: golkom
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