| Literature DB >> 29802667 |
Caicai Meng1, Aniruddha Sasmal2, Yan Zhang1, Tian Gao1,3, Chang-Cheng Liu1,3, Naazneen Khan2, Ajit Varki2, Fengshan Wang1, Hongzhi Cao1,3.
Abstract
O-Mannose glycans account up to 30 % of total O-glycans in the brain. Previous synthesis and functional studies have only focused on the core M3 O-mannose glycans of α-dystroglycan, which are a causative factor for various muscular diseases. In this study, a highly efficient chemoenzymatic strategy was developed that enabled the first collective synthesis of 63 core M1 and core M2 O-mannose glycans. This chemoenzymatic strategy features the gram-scale chemical synthesis of five judiciously designed core structures, and the diversity-oriented modification of the core structures with three enzyme modules to provide 58 complex O-mannose glycans in a linear sequence that does not exceed four steps. The binding profiles of synthetic O-mannose glycans with a panel of lectins, antibodies, and brain proteins were also explored by using a printed O-mannose glycan array.Entities:
Keywords: O-mannose glycans; chemoenzymatic synthesis; dystroglycan; glycosylation; glycosyltransferases
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Year: 2018 PMID: 29802667 PMCID: PMC6176721 DOI: 10.1002/anie.201804373
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336