Characterization of vascular endothelial cell growth factor interactions with the kinase insert domain-containing receptor tyrosine kinase. A real time kinetic study

Abstract

The kinase insert domain-containing receptor (KDR) tyrosine kinase mediates calcium mobilization in endothelial cells and plays a key role during physiological and pathological angiogenesis. To provide a detailed understanding of how KDR is activated, we analyzed the kinetics of ligand- receptor interaction using BIAcore. Both predimerized (KDR-Fc) and monomeric (KDR-cbu) receptors were examined with vascular endothelial cell growth factor (VEGF) homodimers and VEGF/placental growth factor (PlGF) heterodimers. VEGF binds to KDR-Fc with k(a) = 3.6 ± 0.07e6, k(d) = 1.34 ± 0.19e-4, and K(D) = 37.1 ± 4.9 pM. These values are similar to those displayed by monomeric KDR where kα = 5.23 ± 1.4e6, k(d) = 2.74 ± 0.76e-4, and K(D) = 51.7 ± 5.8 pM were apparent. In contrast, VEGF/P1GF bound to KDR-Fc with kα = 7.3 ± 1.6e4, k(d) = 4.4 ± 1.2e-4, and K(D) = 6 ± 1.2 nM. Thus, the heterodimer displays a 160-fold reduced K(D) for binding to predimerized KDR, which is mainly a consequence of a 50-fold reduction in kα. We were unable to detect association between VEGF/PlGF and monomeric KDR. However, nanomolar concentrations of VEGF/PlGF were able to elicit weak calcium mobilization in endothelial cells. This latter observation may indicate partial predimerization of KDR on the cell surface or facilitation of binding due to accessory receptors.