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Visualization of O-GlcNAc glycosylation stoichiometry and dynamics using resolvable poly(ethylene glycol) mass tags.

Authors :
Clark PM
Rexach JE
Hsieh-Wilson LC
Source :
Current protocols in chemical biology [Curr Protoc Chem Biol] 2013; Vol. 5 (4), pp. 281-302.
Publication Year :
2013

Abstract

O-linked N-acetylglucosamine (O-GlcNAc) glycosylation is a dynamic protein posttranslational modification with roles in processes such as transcription, cell cycle regulation, and metabolism. Detailed mechanistic studies of O-GlcNAc have been hindered by a lack of methods for measuring O-GlcNAc stoichiometries and the interplay of glycosylation with other posttranslational modifications. We recently developed a method for labeling O-GlcNAc-modified proteins with resolvable poly(ethylene glycol) mass tags. This mass-tagging approach enables the direct measurement of glycosylation stoichiometries and the visualization of distinct O-GlcNAc-modified subpopulations. Here, we describe procedures for labeling O-GlcNAc glycoproteins in cell lysates with mass tags.

Details

Language :
English
ISSN :
2160-4762
Volume :
5
Issue :
4
Database :
MEDLINE
Journal :
Current protocols in chemical biology
Publication Type :
Academic Journal
Accession number :
24391098
Full Text :
https://doi.org/10.1002/9780470559277.ch130153