Structural and mechanistic characterization of bifunctional heparan sulfate N-deacetylase-N-sulfotransferase 1

Mycroft-West, Courtney J.; Abdelkarim, Sahar; Duyvesteyn, Helen M. E.; Gandhi, Neha S.; Skidmore, Mark A.; Owens, Raymond J.; Wu, Liang

Abstract

Heparan sulfate (HS) polysaccharides are major constituents of the extracellular matrix, which are involved in myriad structural and signaling processes. Mature HS polysaccharides contain complex, non-templated patterns of sulfation and epimerization, which mediate interactions with diverse protein partners. Complex HS modifications form around initial clusters of glucosamine-N-sulfate (GlcNS) on nascent polysaccharide chains, but the mechanistic basis underpinning incorporation of GlcNS itself into HS remains unclear. Here, we determine cryo-electron microscopy structures of human N-deacetylase-N-sulfotransferase (NDST)1, the bifunctional enzyme primarily responsible for initial GlcNS modification of HS. Our structures reveal the architecture of both NDST1 deacetylase and sulfotransferase catalytic domains, alongside a non-catalytic N-terminal domain. The two catalytic domains of NDST1 adopt a distinct back-to-back topology that limits direct cooperativity. Binding analyses, aided by activity-modulating nanobodies, suggest that anchoring of the substrate at the sulfotransferase domain initiates the NDST1 catalytic cycle, providing a plausible mechanism for cooperativity despite spatial domain separation. Our data shed light on key determinants of NDST1 activity, and describe tools to probe NDST1 function in vitro and in vivo.

Citation

Mycroft-West, C. J., Abdelkarim, S., Duyvesteyn, H. M. E., Gandhi, N. S., Skidmore, M. A., Owens, R. J., & Wu, L. (in press). Structural and mechanistic characterization of bifunctional heparan sulfate N-deacetylase-N-sulfotransferase 1. Nature Communications, 15(1), Article 1326. https://doi.org/10.1038/s41467-024-45419-4

• Journal Article Type: Article
• Acceptance Date: Jan 22, 2024
• Online Publication Date: Feb 13, 2024
• Deposit Date: Mar 4, 2024
• Journal: Nature Communications
• Publisher: Nature Publishing Group
• Peer Reviewed: Peer Reviewed
• Volume: 15
• Issue: 1
• Article Number: 1326
• DOI: https://doi.org/10.1038/s41467-024-45419-4
• Publisher URL: https://www.nature.com/articles/s41467-024-45419-4