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Chemoenzymatic Assembly of Mammalian O-Mannose Glycans.

Caicai MengAniruddha SasmalYan ZhangTian GaoChang-Cheng LiuNaazneen KhanAjit VarkiFengshan WangHong-Zhi Cao
Published in: Angewandte Chemie (International ed. in English) (2018)
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.
Keyphrases
  • cell surface
  • highly efficient
  • high resolution
  • resting state
  • white matter
  • functional connectivity
  • mass spectrometry
  • body composition
  • resistance training
  • gram negative
  • subarachnoid hemorrhage
  • high density