1. Academic Validation
  2. Antibodies and activity measurements for the detection of O-GlcNAc transferase and assay of its substrate, UDP-GlcNAc

Antibodies and activity measurements for the detection of O-GlcNAc transferase and assay of its substrate, UDP-GlcNAc

  • Methods Mol Biol. 2013;1022:147-59. doi: 10.1007/978-1-62703-465-4_12.
Tony Lefebvre 1 Ludivine Drougat Stephanie Olivier-Van Stichelen Jean-Claude Michalski Anne-Sophie Vercoutter-Edouart
Affiliations

Affiliation

  • 1 Unit of Structural and Functional Glycobiology, University of Lille 1, Villeneuve d'Ascq, France.
Abstract

Since the discovery of O-GlcNAc modification (O-GlcNAcylation) 20 years ago, much attention has been given to OGT (O-GlcNAc transferase), the unique Enzyme responsible for the nuclear and cytosolic O-GlcNAcylation processes. This review focuses on protocols that are routinely used to analyze OGT expression and activity. First are detailed techniques using rabbit polyclonal anti-OGT Antibodies, namely, Western blot, (co-)immunoprecipitation, and immunofluorescence. We also describe the measurement of OGT activity by using synthetic Peptides as acceptors and radiolabeled UDP-GlcNAc. Finally, a sensitive HPAEC-based technique to measure the cellular content of UDP-GlcNAc, the donor substrate of OGT, is described in detail.

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