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Xyloside Derivatives as Molecular Tools to Selectively Inhibit Heparan Sulfate and Chondroitin Sulfate Proteoglycan Biosynthesis.
Mencio, Caitlin; Balagurunathan, Kuberan; Koketsu, Mamoru.
Affiliation
  • Mencio C; Interdepartmental Program in Neuroscience, University of Utah, Salt Lake City, UT, USA.
  • Balagurunathan K; Departments of Biology, Bioengineering, & Medicinal Chemistry, University of Utah, Salt Lake City, UT, USA.
  • Koketsu M; Department of Chemistry and Biomolecular Science, Faculty of Engineering, Gifu University, Gifu, Japan. koketsu@gifu-u.ac.jp.
Methods Mol Biol ; 2303: 753-764, 2022.
Article in En | MEDLINE | ID: mdl-34626420
Glycosaminoglycan (GAG) side chains of proteoglycans are involved in a wide variety of developmental and pathophysiological functions. Similar to a gene knockout, the ability to inhibit GAG biosynthesis would allow us to examine the function of endogenous GAG chains. However, ubiquitously and irreversibly knocking out all GAG biosynthesis would cause multiple effects, making it difficult to attribute a specific biological role to a specific GAG structure in spatiotemporal manner. Reversible and selective inhibition of GAG biosynthesis would allow us to examine the importance of endogenous GAGs to specific cellular, tissue, or organ systems. In this chapter, we describe the chemical synthesis and biological evaluation of xyloside derivatives as selective inhibitors of heparan sulfate and chondroitin/dermatan sulfate proteoglycan biosynthesis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycosides Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycosides Language: En Journal: Methods Mol Biol Journal subject: BIOLOGIA MOLECULAR Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States