Processing of GB virus B non-structural proteins in cultured cells requires both NS3 protease and NS4A cofactor

J Gen Virol. 2000 Sep;81(Pt 9):2183-2188. doi: 10.1099/0022-1317-81-9-2183.

Abstract

The identification of antivirals and vaccines against hepatitis C virus (HCV) infection is hampered by the lack of convenient animal models. The need to develop surrogate models has recently drawn attention to GB virus B (GBV-B), which produces hepatitis in small primates. In a previous study in vitro, it was shown that GBV-B NS3 protease shares substrate specificity with the HCV enzyme, known to be crucial for virus replication. In this report, GBV-B NS3 activity on GBV-B precursor proteins has been analysed in a cell-based system. It is shown that mature protein products are obtained that are compatible with the cleavage sites proposed on the basis of sequence homology with HCV and that GBV-B NS4A protein is required as a cofactor for optimal enzymatic activity. Experiments in vitro supported by a structural model mapped the region of NS4A that interacts with NS3 and showed that the GBV-B cofactor cannot be substituted for by its HCV analogue.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antigens, Viral / metabolism*
  • Cebidae
  • Cells, Cultured
  • Flaviviridae / physiology*
  • Hepacivirus / physiology
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Sorting Signals
  • RNA Helicases / metabolism*
  • Serine Endopeptidases / metabolism*
  • Structure-Activity Relationship
  • Substrate Specificity
  • Viral Nonstructural Proteins / metabolism*
  • Virus Replication

Substances

  • Antigens, Viral
  • NS3 protein, flavivirus
  • NS4A protein, flavivirus
  • Protein Sorting Signals
  • Viral Nonstructural Proteins
  • Serine Endopeptidases
  • RNA Helicases