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An enzymatic strategy to asymmetrically branched N-glycans.
Calderon, Angie D; Zhou, Jun; Guan, Wanyi; Wu, Zhigang; Guo, Yuxi; Bai, Jing; Li, Qing; Wang, Peng George; Fang, Junqiang; Li, Lei.
Affiliation
  • Calderon AD; Department of Chemistry and Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, GA 30303, USA. lli22@gsu.edu.
Org Biomol Chem ; 15(35): 7258-7262, 2017 Sep 13.
Article in En | MEDLINE | ID: mdl-28832049
ABSTRACT
An enzymatic strategy was developed to generate asymmetrically branched N-glycans from natural sources by using a panel of glycosidases and glycosyltransferases. Briefly, LacZ ß-galactosidase was employed to selectively trim symmetrically branched N-glycans isolated from bovine fetuin. The yielding structures were then converted to asymmetrically branched core structures by robust glycosyltransferase for further extension.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Glycosyltransferases / Beta-Galactosidase Limits: Animals Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2017 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Glycosyltransferases / Beta-Galactosidase Limits: Animals Language: En Journal: Org Biomol Chem Journal subject: BIOQUIMICA / QUIMICA Year: 2017 Document type: Article Affiliation country: United States