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dc.contributor.authorHu, Yu-Pengen_US
dc.contributor.authorZhong, Yong-Qingen_US
dc.contributor.authorChen, Zhi-Gengen_US
dc.contributor.authorChen, Chun-Yenen_US
dc.contributor.authorShi, Zhonghaoen_US
dc.contributor.authorZulueta, Medel Manuel L.en_US
dc.contributor.authorKu, Chiao-Chuen_US
dc.contributor.authorLee, Pei-Yingen_US
dc.contributor.authorWang, Cheng-Chungen_US
dc.contributor.authorHung, Shang-Chengen_US
dc.date.accessioned2014-12-08T15:29:00Z-
dc.date.available2014-12-08T15:29:00Z-
dc.date.issued2012-12-26en_US
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ja3090065en_US
dc.identifier.urihttp://hdl.handle.net/11536/20917-
dc.description.abstractSeveral biological processes involve glycans, yet understanding their ligand specificities is impeded by their inherent diversity and difficult acquisition. Generating broad synthetic sugar libraries for bioevaluations is a powerful tool in unraveling glycan structural information. In the case of the widely distributed heparan sulfate (HS), however, the 48 theoretical possibilities for its repeating disaccharide call for synthetic approaches that should minimize the effort in an undoubtedly huge undertaking. Here we employed a divergent strategy to afford all 48 HS-based disaccharides from just two orthogonally protected disaccharide precursors. Different combinations and sequence of transformation steps were applied with many downstream intermediates leading up to multiple target products. With the full disaccharide library in hand, affinity screening with fibroblast growth factor-1 (FGF-1) revealed that four of the synthetic sugars bind to FGF-1. The molecular details of the interaction were further clarified through X-ray analysis of the sugar-protein cocrystals. The capability of comprehensive sugar libraries in providing key insights in glycan-ligand interaction is, thus, highlighted.en_US
dc.language.isoen_USen_US
dc.titleDivergent Synthesis of 48 Heparan Sulfate-Based Disaccharides and Probing the Specific Sugar-Fibroblast Growth Factor-1 Interactionen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ja3090065en_US
dc.identifier.journalJOURNAL OF THE AMERICAN CHEMICAL SOCIETYen_US
dc.citation.volume134en_US
dc.citation.issue51en_US
dc.citation.spage20722en_US
dc.citation.epage20727en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000313154200027-
dc.citation.woscount10-
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