| Literature DB >> 28092045 |
Mi Ke1, Bizhu Chu1, Lin Lin1,2, Ruijun Tian3,4.
Abstract
Dynamic tyrosine phosphorylation is a key molecular modulation for many signal transduction events. Because of their low abundance and dynamic nature in cells, the detection and enrichment of phosphotyrosine proteins has long relied on specific antibodies, such as 4G10 and P-Tyr-100. Another well-established approach for phosphotyrosine proteins recognition and enrichment is by their specific binding domains, such as Src homology 2 (SH2) domains. In this chapter, we describe a typical analytical approach for purifying specific SH2 domains, enriching specific phosphotyrosine proteins from activated cells, mass spectrometry analysis, and related data analysis.Entities:
Keywords: Affinity reagent; LC-MS; Phosphotyrosine; Proteomics; SH2 domain; Signal transduction
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Year: 2017 PMID: 28092045 DOI: 10.1007/978-1-4939-6762-9_22
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745