| Literature DB >> 27529638 |
Zhigang Wu1, Kuan Jiang2,1, Hailiang Zhu1, Cheng Ma1, Zaikuan Yu1, Lei Li1, Wanyi Guan1,3, Yunpeng Liu1, He Zhu1, Yanyi Chen1, Shanshan Li1, Jing Li2,1, Jiansong Cheng2, Lianwen Zhang2, Peng George Wang2,1.
Abstract
Here we report a facile and efficient method for site-directed glycosylation of peptide/protein. The method contains two sequential steps: generation of a GlcNAc-O-peptide/protein, and subsequent ligation of a eukaryotic N-glycan to the GlcNAc moiety. A pharmaceutical peptide, glucagon-like peptide-1 (GLP-1), and a model protein, bovine α-Crystallin, were successfully glycosylated using such an approach. It was shown that the GLP-1 with O-linked N-glycan maintained an unchanged secondary structure after glycosylation, suggesting the potential application of this approach for peptide/protein drug production. In summary, the coupled approach provides a general strategy to produce homogeneous glycopeptide/glycoprotein bearing eukaryotic N-glycans.Entities:
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Year: 2016 PMID: 27529638 PMCID: PMC5951161 DOI: 10.1021/acs.bioconjchem.6b00385
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774