Synthesis of oligomeric mannosides and their structure-binding relationship with concanavalin A

Chem Asian J. 2014 Jul;9(7):1786-96. doi: 10.1002/asia.201402029. Epub 2014 May 5.

Abstract

Small glycodendrimers with α-mannosyl ligands were synthesized by using copper-catalyzed azide-alkyne coupling chemistry and some of these molecules were used as multivalent ligands to study the induction of concanavalin A (Con A) precipitation. The results showed that the monovalent mannose ligand could induce the precipitation of Con A. This unexpected finding initiated a series of studies to characterize the molecular basis of the ligand-lectin interaction. The atypical precipitation is found to be specific to the mannose, fluorescein moiety (FITC), and Con A. Apparently the mannose ligand binds to Con A through hydrogen-bonding interactions, whereas the binding of FITC is mediated by hydrophobic forces.

Keywords: carbohydrates; dendrimers; glycopeptides; multivalent effect; precipitation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Chemical Precipitation
  • Chemistry Techniques, Synthetic
  • Concanavalin A / chemistry
  • Concanavalin A / metabolism*
  • Fluorescein / chemistry
  • Fluorescein / metabolism
  • Fluorescence Polarization
  • Mannosides / chemical synthesis*
  • Mannosides / chemistry
  • Mannosides / metabolism*
  • Scattering, Radiation
  • Structure-Activity Relationship
  • Thermodynamics

Substances

  • Mannosides
  • Concanavalin A
  • Fluorescein