| Literature DB >> 26571101 |
Shisheng Sun1, Punit Shah1, Shadi Toghi Eshghi1, Weiming Yang1, Namita Trikannad1, Shuang Yang1, Lijun Chen1, Paul Aiyetan1, Naseruddin Höti1, Zhen Zhang1, Daniel W Chan1, Hui Zhang1.
Abstract
Comprehensive characterization of protein glycosylation is critical for understanding the structure and function of glycoproteins. However, due to the complexity and heterogeneity of glycoprotein conformations, current glycoprotein analyses focus mainly on either the de-glycosylated glycosylation site (glycosite)-containing peptides or the released glycans. Here, we describe a chemoenzymatic method called solid phase extraction of N-linked glycans and glycosite-containing peptides (NGAG) for the comprehensive characterization of glycoproteins that is able to determine glycan heterogeneity for individual glycosites in addition to providing information about the total N-linked glycan, glycosite-containing peptide and glycoprotein content of complex samples. The NGAG method can also be applied to quantitatively detect glycoprotein alterations in total and site-specific glycan occupancies.Entities:
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Year: 2015 PMID: 26571101 PMCID: PMC4872599 DOI: 10.1038/nbt.3403
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908