| Literature DB >> 24391098 |
Peter M Clark1, Jessica E Rexach, Linda C Hsieh-Wilson.
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.Entities:
Keywords: O-linked N-acetylglucosamine; chemoenzymatic labeling; glycosylation; poly(ethylene glycol); posttranslational modifications; protein subpopulations
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Year: 2013 PMID: 24391098 PMCID: PMC3931299 DOI: 10.1002/9780470559277.ch130153
Source DB: PubMed Journal: Curr Protoc Chem Biol ISSN: 2160-4762