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Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling
Published on: February 5, 2018
Divergent Enzymatic Synthesis of a Comprehensive Type‑1 Glycan Determinant Library
Guitao Bai1, Tangliang Shen1, MohammadHossein Shabahang1
1Department of Chemistry and Center for Diagnostics & Therapeutics, Georgia State University, Atlanta, Georgia 30303, United States.
Abstract:
Type-1 glycan unit, Galβ1-3GlcNAc, is one of the two major backbones from which the large glycan determinant repertoire is derived. Numerous type-1 glycan determinants, including Lewis-series antigens, have been identified, often featuring fucosylation and sialylation. In this study, we achieved efficient synthesis of 30 type-1 determinants using a divergent enzymatic strategy. The synthetic efficiency of eight fucosyltransferases (FucTs) was evaluated for the installation of fucose at every step of the type-1 determinant synthesis. Using selected FucTs and a few additional robust glycosyltransferases, 22 basic type-1 determinants were constructed at preparative scales in no more than three steps, starting from the type-1 unit. Additionally, 8 extended type-1 Lewis antigens were successfully synthesized in no more than five steps. Subsequent glycan microarray assays of these glycan determinants revealed intriguing recognitions by glycan-binding proteins and anti-type-1 Lewis antigen monoclonal antibodies.
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