Structure of the Reovirus Membrane-Penetration Protein, Mu1, in a Complex With Is Protector Protein, Sigma3

Cell. 2002 Jan 25;108(2):283-95. doi: 10.1016/s0092-8674(02)00612-8.

Abstract

Cell entry by nonenveloped animal viruses requires membrane penetration without membrane fusion. The reovirus penetration agent is the outer-capsid protein, Mu1. The structure of Mu1, complexed with its "protector" protein, Sigma3, and the fit of this Mu1(3)Sigma3(3) heterohexameric complex into the cryoEM image of an intact virion, reveal molecular events essential for viral penetration. Autolytic cleavage divides Mu1 into myristoylated Mu1N and Mu1C. A long hydrophobic pocket can receive the myristoyl group. Dissociation of Mu1N, linked to a major conformational change of the entire Mu1 trimer, must precede myristoyl-group insertion into the cellular membrane. A myristoyl switch, coupling exposure of the fatty acid chain, autolytic cleavage of Mu1N, and long-range molecular rearrangement of Mu1C, thus appears to be part of the penetration mechanism.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Capsid / chemistry*
  • Capsid / isolation & purification
  • Capsid / metabolism
  • Capsid Proteins*
  • Crystallography, X-Ray
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Structure, Tertiary*
  • Protein Subunits
  • RNA-Binding Proteins / chemistry
  • RNA-Binding Proteins / isolation & purification
  • RNA-Binding Proteins / metabolism
  • Reoviridae / physiology*
  • Sequence Alignment
  • Viral Proteins / chemistry
  • Viral Proteins / isolation & purification
  • Viral Proteins / metabolism
  • Virion / chemistry
  • Virion / ultrastructure

Substances

  • Capsid Proteins
  • Protein Subunits
  • RNA-Binding Proteins
  • Viral Proteins
  • mu1 protein, Reovirus
  • sigma protein 3, Reovirus

Associated data

  • PDB/1JMU