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Visualization of O-GlcNAc glycosylation stoichiometry and dynamics using resolvable poly(ethylene glycol) mass tags.
- 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.
- Subjects :
- Animals
Azides chemistry
Carbohydrate Sequence
Cycloaddition Reaction methods
Galactosyltransferases chemistry
Galactosyltransferases genetics
Humans
Molecular Sequence Data
Oximes metabolism
Protein Processing, Post-Translational genetics
Proteins chemistry
Acetylglucosamine metabolism
Glycosylation drug effects
Polyethylene Glycols pharmacology
Subjects
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