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.

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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
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article

Merging Enzymatic Catalysis with Iron Catalysis for Highly Stereoselective Heparan Sulfate Oligosaccharide Assembly

Pinzhi Wang, Changmin Xie, Xiao-Wen Zhang, Hao Xu et al.
2 citations
Journal of the American Chemical Society
Proteoglycans and glycosaminoglycans research
2.30
article

Merging Enzymatic Catalysis with Iron Catalysis for Highly Stereoselective Heparan Sulfate Oligosaccharide Assembly

Pinzhi Wang, Changmin Xie, Xiao-Wen Zhang, Hao Xu, Eduardo Stancanelli, Haoran Wang, Junjiang Sun, Dakang Zhang, Jian Liu, Yongmei Xu, Zixiang Jiang, Haoyu Yang, Le Yin
article en
2 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 148(1)
G1 Therapeutics (United States) (US), Brandeis University (US)
Clean water and sanitation
Openalex Percentile: Top 11%
Proteoglycans and glycosaminoglycans research
2.30
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