Literature DB >> 28092045

SH2 Domains as Affinity Reagents for Phosphotyrosine Protein Enrichment and Proteomic Analysis.

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


  1 in total

1.  Exploring protein phosphorylation by combining computational approaches and biochemical methods.

Authors:  Gonzalo Pérez-Mejías; Alejandro Velázquez-Cruz; Alejandra Guerra-Castellano; Blanca Baños-Jaime; Antonio Díaz-Quintana; Katiuska González-Arzola; Miguel Ángel De la Rosa; Irene Díaz-Moreno
Journal:  Comput Struct Biotechnol J       Date:  2020-07-07       Impact factor: 7.271

  1 in total

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