Recombinant hepatitis E capsid protein self-assembles into a dual-domain T = 1 particle presenting native virus epitopes

Virology. 1999 Dec 5;265(1):35-45. doi: 10.1006/viro.1999.0005.

Abstract

The three-dimensional structure of a self-assembled, recombinant hepatitis E virus particle has been solved to 22-A resolution by cryo-electron microscopy and three-dimensional image reconstruction. The single subunit of 50 kDa is derived from a truncated version of the open reading frame-2 gene of the virus expressed in a baculovirus system. This is the first structure of a T = 1 particle with protruding dimers at the icosahedral two-fold axes solved by cryo-electron microscopy. The protein shell of these hollow particles extends from a radius of 50 A outward to a radius of 135 A. In the reconstruction, the capsid is dominated by dimers that define the 30 morphological units. The outer domain of the homodimer forms a protrusion, which corresponds to the spike-like density seen in the cryo-electron micrograph. This particle retains native virus epitopes, suggesting its potential value as a vaccine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Capsid / ultrastructure*
  • Cryoelectron Microscopy
  • Epitopes / ultrastructure
  • Hepatitis E virus / ultrastructure*
  • Image Processing, Computer-Assisted
  • Models, Molecular
  • Molecular Weight
  • Protein Conformation
  • Protein Folding
  • Recombinant Proteins / ultrastructure
  • Virion / ultrastructure

Substances

  • Epitopes
  • Recombinant Proteins