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Poly-N-Acetyllactosamine Neo-Glycoproteins as Nanomolar Ligands of Human Galectin-3: Binding Kinetics and Modeling.

Abstract
Galectin-3 (Gal-3) is recognized as a prognostic marker in several cancer types. Its involvement in tumor development and proliferation makes this lectin a promising target for early cancer diagnosis and anti-cancer therapies. Gal-3 recognizes poly-N-acetyllactosamine (LacNAc)-based carbohydrate motifs of glycoproteins and glycolipids with a high specificity for internal LacNAc epitopes. This study analyzes the mode and kinetics of binding of Gal-3 to a series of multivalent neo-glycoproteins presenting complex poly-LacNAc-based oligosaccharide ligands on a scaffold of bovine serum albumin. These neo-glycoproteins rank among the strongest Gal-3 ligands reported, with Kd reaching sub-nanomolar values as determined by surface plasmon resonance. Significant differences in the binding kinetics were observed within the ligand series, showing the tetrasaccharide capped with N,N'-diacetyllactosamine (LacdiNAc) as the strongest ligand of Gal-3 in this study. A molecular model of the Gal-3 carbohydrate recognition domain with docked oligosaccharide ligands is presented that shows the relations in the binding site at the molecular level. The neo-glycoproteins presented herein may be applied for selective recognition of Gal-3 both on the cell surface and in blood serum.
AuthorsLadislav Bumba, Dominic Laaf, Vojtěch Spiwok, Lothar Elling, Vladimír Křen, Pavla Bojarová
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 19 Issue 2 (Jan 26 2018) ISSN: 1422-0067 [Electronic] Switzerland
PMID29373511 (Publication Type: Journal Article)
Chemical References
  • Galectin 3
  • Glycoproteins
  • Ligands
  • N-acetylgalactosaminyl-1-4-N-acetylglucosamine
  • Serum Albumin, Bovine
  • Lactose
Topics
  • Binding Sites
  • Galectin 3 (chemistry, metabolism)
  • Glycoproteins (chemistry, pharmacology)
  • Humans
  • Lactose (analogs & derivatives, chemistry)
  • Ligands
  • Molecular Docking Simulation
  • Protein Binding
  • Serum Albumin, Bovine (chemistry)

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