| Literature DB >> 26066578 |
Abstract
Protein glycosylation is one of the most important protein modifications. Glycosylation site occupancy alteration has been implicated in human diseases and cancers. However, current glycoproteomic methods focus on the identification and quantification of glycosylated peptides and glycosylation sites but not glycosylation occupancy or glycoform stoichiometry. Here we describe a method for large-scale determination of the absolute glycosylation stoichiometry using three independent relative ratios. Using this method, we determined 117 absolute N-glycosylation occupancies in OVCAR-3 cells. Finally, we investigated the possible functions and the determinants for partial glycosylation.Entities:
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Year: 2015 PMID: 26066578 PMCID: PMC4729197 DOI: 10.1021/acs.analchem.5b01679
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986