Distinct cellular receptor interactions in poliovirus and rhinoviruses

EMBO J. 2000 Mar 15;19(6):1207-16. doi: 10.1093/emboj/19.6.1207.

Abstract

Receptor binding to human poliovirus type 1 (PV1/M) and the major group of human rhinoviruses (HRV) was studied comparatively to uncover the evolution of receptor recognition in picornaviruses. Surface plas- mon resonance showed receptor binding to PV1/M with faster association and dissociation rates than to HRV3 and HRV16, two serotypes that have similar binding kinetics. The faster rate for receptor association to PV1/M suggested a relatively more accessible binding site. Thermodynamics for receptor binding to the viruses and assays for receptor-mediated virus uncoating showed a more disruptive receptor interaction with PV1/M than with HRV3 or HRV16. Cryo-electron microscopy and image reconstruction of receptor-PV1/M complexes revealed receptor binding to the 'wall' of surface protrusions surrounding the 'canyon', a depressive surface in the capsid where the rhinovirus receptor binds. These data reveal more exposed receptor-binding sites in poliovirus than rhinoviruses, which are less protected from immune surveillance but more suited for receptor-mediated virus uncoating and entry at the cell surface.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Capsid / metabolism
  • Capsid / ultrastructure
  • Cell Line
  • Cryoelectron Microscopy
  • Humans
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism
  • Intercellular Adhesion Molecule-1 / ultrastructure
  • Kinetics
  • Membrane Proteins*
  • Models, Biological
  • Models, Molecular
  • Peptide Fragments / genetics
  • Peptide Fragments / metabolism
  • Peptide Fragments / ultrastructure
  • Poliovirus / chemistry
  • Poliovirus / metabolism*
  • Poliovirus / physiology
  • Poliovirus / ultrastructure
  • Protein Conformation
  • Receptors, Virus / genetics
  • Receptors, Virus / metabolism*
  • Receptors, Virus / ultrastructure
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / ultrastructure
  • Rhinovirus / chemistry
  • Rhinovirus / metabolism*
  • Rhinovirus / physiology
  • Rhinovirus / ultrastructure
  • Solubility
  • Substrate Specificity
  • Surface Plasmon Resonance
  • Temperature
  • Thermodynamics

Substances

  • Membrane Proteins
  • Peptide Fragments
  • Receptors, Virus
  • Recombinant Proteins
  • poliovirus receptor
  • Intercellular Adhesion Molecule-1