Phosphoprotein enrichment for protein analysis in motile T-lymphocytes

Praseetha Prasannan*, Rathi Saravanan, Navin Kumar Verma

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Protein phosphorylation plays a key role in intracellular signal transduction and regulates diverse cellular functions. This posttranslational modification of proteins occurs dynamically and reversibly and only a small fraction of the total proteins is phosphorylated at any given time depending on the cell types and their functioning. Thus, a relatively low abundance of phosphorylated proteins is present in specific cells under certain conditions and hence it becomes problematic to detect these proteins and their analysis. In particular, phosphoproteomic analysis of rapidly migrating T-lymphocytes is always challenging. In order to analyze phosphoproteins in motile T-cells using techniques such as polyacrylamide gel electrophoresis and mass spectrometry, it is often important to enrich the phosphorylated forms in the cellular lysates. In this chapter, we describe a simple method to enrich phosphoproteins that can be used for protein analysis in motile T-cells.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages83-90
Number of pages8
DOIs
Publication statusPublished - 2019
Externally publishedYes

Publication series

NameMethods in Molecular Biology
Volume1930
ISSN (Print)1064-3745

Bibliographical note

Publisher Copyright:
© 2019, Springer Science+Business Media, LLC, part of Springer Nature.

ASJC Scopus Subject Areas

  • Molecular Biology
  • Genetics

Keywords

  • Mass spectrometry
  • Phosphoproteomics
  • Protein phosphorylation
  • T-cell migration

Fingerprint

Dive into the research topics of 'Phosphoprotein enrichment for protein analysis in motile T-lymphocytes'. Together they form a unique fingerprint.

Cite this