| Literature DB >> 27454154 |
Peter V Robinson1,2, Cheng-Ting Tsai1,2, Amber E de Groot1,2, Julia L McKechnie1,2, Carolyn R Bertozzi1,2.
Abstract
We report a non-destructive biochemical technique, termed "Glyco-seek", for analysis of O-GlcNAcylated proteins. Glyco-seek combines chemoenzymatic labeling, proximity ligation, and quantitative polymerase chain reaction to detect O-GlcNAcylated proteins with ultrahigh sensitivity. Our glycan-specific assay can be paired with traditional proximity ligation assays to simultaneously determine the change in total protein levels. We show that Glyco-seek detects attomoles of glycoproteins of interest from cell lysates, with sensitivity several orders of magnitude higher than that of current techniques. We used the method to directly assay the O-GlcNAcylation status of a low-abundance transcription factor from cell lysates without need for isolation or enrichment.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27454154 PMCID: PMC5327792 DOI: 10.1021/jacs.6b03861
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419