Literature DB >> 29802667

Chemoenzymatic Assembly of Mammalian O-Mannose Glycans.

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.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  O-mannose glycans; chemoenzymatic synthesis; dystroglycan; glycosylation; glycosyltransferases

Mesh:

Substances:

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


  37 in total

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