Molecular force spectroscopy of homophilic nectin-1 interactions

Biochem Biophys Res Commun. 2007 Nov 3;362(4):886-92. doi: 10.1016/j.bbrc.2007.08.096. Epub 2007 Aug 28.

Abstract

Nectins are Ca2+ independent cell adhesion molecules localizing at the cadherin based adherens junctions. In this study, we have used atomic force microscopy to study interaction of a chimera of extra cellular fragment of nectin-1 and Fc of human IgG (nef-1) with wild type L-fibroblasts that express endogenous nectin-1 to elucidate the biophysical characteristics of homophilic nectin-1 trans-interactions at the level of single molecule. Bond strength distribution revealed three distinct bound states (or configurations) of trans-interactions between paired nectins, where each bound state has a unique unstressed off-rate and reactive compliance. Kinetic analysis of force-dependent off-rate of the bound state involving trans-interacting V-V domains between paired nectin-1 (unstressed off-rate approximately 1.465+/-0.779 s(-1), reactive compliance approximately 0.143+/-0.072 nm) was found to be closest to E-cadherin, indicating that V-V domain trans-interactions are probably necessary to initiate and promote adhesions of E-cadherin at adherens junctions (AJs).

MeSH terms

  • Cell Adhesion Molecules / metabolism*
  • Cell Line
  • Fibroblasts / metabolism*
  • Microscopy, Atomic Force / methods*
  • Nectins
  • Protein Binding
  • Receptors, HIV / metabolism*
  • Stress, Mechanical

Substances

  • Cell Adhesion Molecules
  • NECTIN1 protein, human
  • Nectins
  • Nef receptor
  • Receptors, HIV