Proteolytic activity of NS3 serine proteinase of hepatitis C virus efficiently expressed in Escherichia coli

Hepatology. 1995 Dec;22(6):1648-55.

Abstract

The serine proteinase of hepatitis C virus (HCV) non-structural protein NS3 was efficiently expressed in an active form as a fused protein with oligohistidine in Escherichia coli. The recombinant fusion protein was purified to near homogeneity by affinity chromatography on a metal chelation column. Trans-cleavage activity of this protein was investigated by using the substrate NS5 protein expressed in insect cells. The purified serine proteinase trans-cleaved the partially purified NS5 protein. In contrast, the NS3 proteins with mutations at the proposed catalytic site, Ser1165 or His1083, lost the trans-cleavage activity. Analysis of the authentic enzyme and variants with site-directed mutations provides a useful tool for understanding the structure-function relationship of the NS3 serine proteinase. We then developed an in vivo trans-cleavage assay system by coexpression of the NS3 proteinase and the NS5 substrate in E coli, and examined the effect of known inhibitors of serine proteinase. Inhibition of its proteolytic activity by N-p-tosyl-L-lysine chloromethyl ketone (TLCK) was observed, but only at high concentrations. The in vitro and in vivo trans-cleavage assays for NS3 serine proteinase will facilitate efficient testing for inhibitors of the replication of HCV and specific treatment for hepatitis C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Baculoviridae / genetics
  • Base Sequence
  • Binding Sites
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Gene Expression*
  • Hepacivirus / enzymology*
  • Histidine / genetics
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Protease Inhibitors / pharmacology
  • Recombinant Fusion Proteins / metabolism
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism*
  • Structure-Activity Relationship
  • Tosyllysine Chloromethyl Ketone / pharmacology
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / metabolism*

Substances

  • NS3 protein, hepatitis C virus
  • Protease Inhibitors
  • Recombinant Fusion Proteins
  • Viral Nonstructural Proteins
  • Tosyllysine Chloromethyl Ketone
  • Histidine
  • NS-5 protein, hepatitis C virus
  • Serine Endopeptidases