Mass Spectrometry-Based Quantitative O-GlcNAcomic Analysis

Methods Mol Biol. 2016:1410:91-103. doi: 10.1007/978-1-4939-3524-6_6.

Abstract

The dynamic co- and post-translational modification (PTM) of proteins, O-linked β-D-N-acetylglucosamine modification (O-GlcNAcylation) of serine/threonine residues is critical in many cellular processes, contributing to multiple physiological and pathological events. The term "O-GlcNAcome" refers to not only the complete set of proteins that undergo O-GlcNAcylation but also the O-GlcNAc status at individual residues, as well as the dynamics of O-GlcNAcylation in response to various stimuli. O-GlcNAcomic analyses have been a challenge for many years. In this chapter, we describe a recently developed approach for the identification and quantification of O-GlcNAc proteins/peptides from complex samples.

Keywords: Chemoenzymatic labeling; Electron transfer dissociation (ETD); GalT1 labeling; O-GlcNAcome; O-GlcNAcylation; Photocleavage; Quantitative mass spectrometry; SILAC; Site mapping.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetylglucosamine / chemistry
  • Glycosylation
  • Humans
  • Mass Spectrometry / methods*
  • Phosphorylation
  • Protein Processing, Post-Translational

Substances

  • Acetylglucosamine