Improved lectin-mediated immobilization of human red blood cells in superporous agarose beads
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Updated: Sep 28, 2026

A Lectin HPLC Method to Enrich Selectively-glycosylated Peptides from Complex Biological Samples
Published on: October 1, 2009
Ingo Gottschalk1, Per Erik Gustavsson, Bo Ersson
1Department of Biochemistry, Biomedical Center, Uppsala University, SE-751 23, Uppsala, Sweden. ingo.gottschalk@biokem.uu.se
Abstract:
A new type of agarose bead, superporous agarose, was used as a gel support for immobilization of human red blood cells (RBCs) mediated by wheat germ lectin. The number of immobilized cells was similar to that obtained with commercial wheat germ lectin-agarose but the cell stability appeared to be superior. This allowed improved frontal affinity chromatographic analyses of cytochalasin B (CB)-binding to the glucose transporter GLUT1 which established a ratio of one CB-binding site per GLUT1 dimer for both plain RBCs or those treated with different poly amino acids. The measured dissociation constants, 70+/-14 nM for CB and 12+/-3 mM for glucose binding to GLUT1, are similar to those reported earlier.

