The crystal structure of coxsackievirus A21 and its interaction with ICAM-1

Structure. 2005 Jul;13(7):1019-33. doi: 10.1016/j.str.2005.04.011.

Abstract

CVA21 and polioviruses both belong to the Enterovirus genus in the family of Picornaviridae, whereas rhinoviruses form a distinct picornavirus genus. Nevertheless, CVA21 and the major group of human rhinoviruses recognize intercellular adhesion molecule-1 (ICAM-1) as their cellular receptor, whereas polioviruses use poliovirus receptor. The crystal structure of CVA21 has been determined to 3.2 A resolution. Its structure has greater similarity to poliovirus structures than to other known picornavirus structures. Cryo-electron microscopy (cryo-EM) was used to determine an 8.0 A resolution structure of CVA21 complexed with an ICAM-1 variant, ICAM-1(Kilifi). The cryo-EM map was fitted with the crystal structures of ICAM-1 and CVA21. Significant differences in the structure of CVA21 with respect to the poliovirus structures account for the inability of ICAM-1 to bind polioviruses. The interface between CVA21 and ICAM-1 has shape and electrostatic complementarity with many residues being conserved among those CVAs that bind ICAM-1.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Capsid
  • Cryoelectron Microscopy
  • Crystallography, X-Ray
  • Dimerization
  • Enterovirus / metabolism*
  • Humans
  • Intercellular Adhesion Molecule-1 / chemistry*
  • Ions
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Protein Binding
  • Sequence Homology, Amino Acid
  • Static Electricity

Substances

  • Ions
  • Intercellular Adhesion Molecule-1

Associated data

  • PDB/1Z7S
  • PDB/1Z7Z
  • PDB/EMD1114