关键词: FDR Heavy methyl SILAC Liquid chromatography-tandem mass spectrometry (LC-MS/MS) Metabolic labeling Protein methylation Protein methyltransferases Proteomics

Mesh : Humans Chromatography, Liquid / methods Tandem Mass Spectrometry / methods Protein Processing, Post-Translational Peptides / chemistry Cell Line Proteome / metabolism Isotope Labeling / methods

来  源:   DOI:10.1007/978-1-0716-2863-8_14

Abstract:
Protein methylation is a widespread post-translational modification (PTM) involved in several important biological processes including, but not limited to, RNA splicing, signal transduction, translation, and DNA repair. Liquid chromatography-tandem mass spectrometry (LC-MS/MS) is considered today the most versatile and accurate technique to profile PTMs with high precision and proteome-wide depth; however, the identification of protein methylations by MS is still prone to high false discovery rates. In this chapter, we describe the heavy methyl SILAC metabolic labeling strategy that allows high-confidence identification of in vivo methyl-peptides by MS-based proteomics. We provide a general protocol that covers the steps of heavy methyl labeling of cultured cells, protein sample preparation, LC-MS/MS analysis, and downstream computational analysis of the acquired MS data.
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