A surface plasmon resonance-based solution affinity assay for heparan sulfate-binding proteins

Glycoconj J. 2009 Jul;26(5):577-87. doi: 10.1007/s10719-008-9210-0. Epub 2008 Nov 26.

Abstract

A surface plasmon resonance-based solution affinity assay is described for measuring the K(d) of binding of heparin/heparan sulfate-binding proteins with a variety of ligands. The assay involves the passage of a pre-equilibrated solution of protein and ligand over a sensor chip onto which heparin has been immobilised. Heparin sensor chips prepared by four different methods, including biotin-streptavidin affinity capture and direct covalent attachment to the chip surface, were successfully used in the assay and gave similar K(d) values. The assay is applicable to a wide variety of heparin/HS-binding proteins of diverse structure and function (e.g., FGF-1, FGF-2, VEGF, IL-8, MCP-2, ATIII, PF4) and to ligands of varying molecular weight and degree of sulfation (e.g., heparin, PI-88, sucrose octasulfate, naphthalene trisulfonate) and is thus well suited for the rapid screening of ligands in drug discovery applications.

MeSH terms

  • Carrier Proteins / metabolism*
  • Chemokine CCL8 / metabolism
  • Fibroblast Growth Factor 1 / metabolism
  • Fibroblast Growth Factor 2 / metabolism
  • Heparitin Sulfate / metabolism*
  • Humans
  • Interleukin-8 / metabolism
  • Protein Binding
  • Surface Plasmon Resonance / methods*
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Carrier Proteins
  • Chemokine CCL8
  • Interleukin-8
  • Vascular Endothelial Growth Factor A
  • Fibroblast Growth Factor 2
  • Fibroblast Growth Factor 1
  • Heparitin Sulfate