Mono-, di- and tri-antennary D-galactose ligands as competitive inhibitors and photoaffinity labels of the hexose transporting system in erythrocytes. A model for the irreversible blocking of receptors in cell membranes

Carbohydr Res. 1995 Oct 16;276(1):57-74. doi: 10.1016/0008-6215(95)00145-j.

Abstract

Starting from pentaerythritol, photolabile mono-, di-, and tri-dentate galactose derivatives as well as their 3H-labelled isotopomers were synthesised. The hydrophilic chains linking the 6 position of D-galactose to pentaerythritol consist of 13 atoms in line. The mono-, di- and tri-dentate compounds, although themselves not transported, inhibit in increasing order 14C-D-galactose transport into erythrocytes. On irradiating whole cells in the presence of ligand with 350-nm UV light, these compounds also in increasing order, could irreversibly block the hexose transport system. Irradiation without ligand has no effect. By using the 3H-labelled tridentate galactose compound the hexose transporter (zone 4.5) is specifically radiolabelled, as could be shown in an SDS-PAGE of membrane proteins from erythrocytes previously photoaffinity labelled. Radiolabelling is significantly suppressed in the presence of D-glucose.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Affinity Labels / chemical synthesis*
  • Affinity Labels / metabolism
  • Binding, Competitive
  • Erythrocyte Membrane / drug effects*
  • Erythrocyte Membrane / metabolism
  • Galactose / analogs & derivatives
  • Galactose / pharmacology*
  • Humans
  • Monosaccharide Transport Proteins / antagonists & inhibitors
  • Monosaccharide Transport Proteins / blood*
  • Receptors, Cell Surface / antagonists & inhibitors*
  • Receptors, Cell Surface / metabolism

Substances

  • Affinity Labels
  • Monosaccharide Transport Proteins
  • Receptors, Cell Surface
  • Galactose