Published October 3, 2022 | Version Submitted + Supplemental Material
Discussion Paper Open

Automated Platform for the Synthesis of Heparan Sulfate Oligosaccharide Libraries for Decoding Glycosaminoglycan-Protein Interactions

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Indiana University Bloomington
  • 3. ROR icon University of North Carolina at Chapel Hill
  • 4. ROR icon Michigan State University

Abstract

Glycosaminoglycans (GAGs) are abundant, ubiquitous carbohydrates in biology, yet their structural complexity has limited an understanding of their biological roles and structure-function relationships. Synthetic access to large collections of well-defined, structurally diverse GAG oligosaccharides would provide critical insights into this important class of biomolecules and represent a major advance in glycoscience. Here, we report a new automated platform for synthesizing heparan sulfate (HS) oligosaccharide libraries displaying comprehensive arrays of sulfation patterns. Library synthesis is made possible by improving the overall synthetic efficiency through universal building blocks derived from natural heparin and a traceless fluorous tagging method for rapid purification and automated synthesis. We used this approach to generate the first comprehensive library of 64 HS tetrasaccharides displaying all possible 2-O-, 6-O-, and N-sulfation sequences. These diverse structures provide an unprecedented view into the sulfation code of GAGs and identify sequences for modulating the activities of important growth factors and chemokines.

Additional Information

The content is available under CC BY NC ND 4.0 License. Financial support was provided by the NIH (U01 GM116262, U01 GM116248 and R44 GM134738) and the Nation Science Foundation (DGE-1745301). We thank Dr. Mona Shahgholi in the CCE Division Mass Spectrometry Facility and Dr. David Vander Velde in the CCE Division NMR Facility at Caltech. M. K. thanks the support of the Graduate Training program in Quantitative and Chemical Biology at Indiana University under the NIH award numbers T32 GM109825 and T32 GM131994. Author contributions. L.W., B-S.H, A.W.S., X.H., J.L., N.L.B.P. and L.C.H-W. designed the research. L.W., B-S.H, A.W.S., M.K. and G.S. performed the research. L.W., B-S.H, A.W.S. and L.C.H-W. wrote the paper. These authors contributed equally: Bo-Shun Huang, Alexander W. Sorum. The authors declare no competing interests.

Attached Files

Submitted - automated-platform-for-the-synthesis-of-heparan-sulfate-oligosaccharide-libraries-for-decoding-glycosaminoglycan-protein-interactions.pdf

Supplemental Material - automated-platform-for-the-synthesis-of-heparan-sulfate-oligosaccharide-libraries-for-decoding-glycosaminoglycan-protein-interactions__1_.pdf

Files

automated-platform-for-the-synthesis-of-heparan-sulfate-oligosaccharide-libraries-for-decoding-glycosaminoglycan-protein-interactions.pdf

Additional details

Additional titles

Alternative title
Efficient Platform for Synthesizing Comprehensive Heparan Sulfate Oligosaccharide Libraries for Decoding Glycosaminoglycan-Protein Interactions

Identifiers

Eprint ID
120403
Resolver ID
CaltechAUTHORS:20230324-457118000.6

Funding

NIH
U01 GM116262
NIH
U01 GM116248
NIH
R44 GM134738
NSF Graduate Research Fellowship
DGE-1745301
NIH Predoctoral Fellowship
T32 GM109825
NIH Predoctoral Fellowship
T32 GM131994

Dates

Created
2023-03-30
Created from EPrint's datestamp field
Updated
2023-07-13
Created from EPrint's last_modified field