Merging Enzymatic Catalysis with Iron Catalysis for Highly Stereoselective Heparan Sulfate Oligosaccharide Assembly
Heparan sulfate (HS) regulates numerous biological processes, but it occurs naturally as a heterogeneous mixture of sulfated complex glycans. Therefore, pursuing a broadly effective approach for homogeneous HS synthesis to advance biological studies has been an outstanding challenge in glycoscience. By merging the catalytic power of sulfotransferases (SULTs) with two distinct iron-catalyzed glycosylation reactions, we report herein a highly stereoselective and generally applicable HS assembly strategy. Every glycosidic linkage in HS was assembled by one of these iron-catalyzed, entirely stereoselective glycosylation reactions. An array of sulfate groups that are essential to HS's function were installed at their desired locations via the SULT-controlled sulfation of HS precursors. This general approach is showcased in the synthesis of an anticoagulant HS hexasaccharide and other full-length precursors of HS octasaccharides.
Authors
- Pinzhi Wang (ORCID: https://orcid.org/0009-0001-8075-4245)
- Changmin Xie (ORCID: https://orcid.org/0000-0003-2808-435X)
- Xiao-Wen Zhang
- Hao Xu (ORCID: https://orcid.org/0000-0002-6069-3246)
- Eduardo Stancanelli (ORCID: https://orcid.org/0000-0002-6006-2209)
- Haoran Wang (ORCID: https://orcid.org/0000-0002-1630-4813)
- Junjiang Sun
- Dakang Zhang
- Jian Liu
- Yongmei Xu
- Zixiang Jiang (ORCID: https://orcid.org/0009-0007-8265-6212)
- Haoyu Yang
- Le Yin
Institutions
- G1 Therapeutics (United States) (US)
- Brandeis University (US)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-12-22
- DOI
- https://doi.org/10.1021/jacs.5c19067
- Citations
- 2
- Primary Topic
- Proteoglycans and glycosaminoglycans research
- Type
- article
- Field-Weighted Citation Impact
- 2.30