4.5 Article

Epimers Switch Galectin-9 Domain Selectivity: 3N-Aryl Galactosides Bind the C-Terminal and Gulosides Bind the N-Terminal

Journal

ACS MEDICINAL CHEMISTRY LETTERS
Volume 11, Issue 1, Pages 34-39

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsmedchemlett.9b00396

Keywords

Galactose; gulose; N-phenyl; epimers; galectin-9; selectivity

Funding

  1. Swedish Research Council [621-2012-2978]
  2. Royal Physiographic Society, Lund
  3. Knut and Alice Wallenberg Foundation [KAW 2013.0022]
  4. Galecto Biotech AB, Lund, Sweden

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A series of 3-deoxy-3-N-arylated-beta-D-galactoside and -guloside derivatives have been synthesized by cesium fluoride/trimetylsilylaryl triflate-mediated benzyne generation and N-arylation of 3-deoxy-3-amino-beta-D-galactosides and -gulosides, respectively. Evaluation as ligands to galectin-1, 2, 3, 4N (N-terminal domain), 4C (C-terminal domain), 7, 8N, 8C, 9C, and 9N revealed that the galactosides selectively bound galectin-9C, whereas the gulosides selectively bound galectin-9N. Hence, the N-aryl group induces galectin-9 selectivity and the ligand 3C-configuration acts as an epimeric selectivity switch between the two domains of galectin-9. Furthermore, MD simulations revealed that galacto derivatives in galectin-9C and gulo derivatives in galectin-9N find stable poses with specific interactions, which proposes a possible explanation to the gal/gulo 9C/9N selectivity.

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