High-throughput screening assay of hepatitis C virus helicase inhibitors using fluorescence-quenching phenomenon

Biochem Biophys Res Commun. 2009 Feb 20;379(4):1054-9. doi: 10.1016/j.bbrc.2009.01.020. Epub 2009 Jan 14.

Abstract

We have developed a novel high-throughput screening assay of hepatitis C virus (HCV) nonstructural protein 3 (NS3) helicase inhibitors using the fluorescence-quenching phenomenon via photoinduced electron transfer between fluorescent dyes and guanine bases. We prepared double-stranded DNA (dsDNA) with a 5'-fluorescent-dye (BODIPY FL)-labeled strand hybridized with a complementary strand, the 3'-end of which has guanine bases. When dsDNA is unwound by helicase, the dye emits fluorescence owing to its release from the guanine bases. Our results demonstrate that this assay is suitable for quantitative assay of HCV NS3 helicase activity and useful for high-throughput screening for inhibitors. Furthermore, we applied this assay to the screening for NS3 helicase inhibitors from cell extracts of microorganisms, and found several cell extracts containing potential inhibitors.

MeSH terms

  • Antiviral Agents / chemistry
  • Antiviral Agents / isolation & purification*
  • Antiviral Agents / pharmacology
  • DNA Helicases / antagonists & inhibitors*
  • Drug Evaluation, Preclinical / methods
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / isolation & purification*
  • Enzyme Inhibitors / pharmacology
  • Fluorescence
  • Fluorescent Dyes / chemistry
  • Hepacivirus / drug effects*
  • Hepacivirus / enzymology
  • Viral Nonstructural Proteins / antagonists & inhibitors*

Substances

  • Antiviral Agents
  • Enzyme Inhibitors
  • Fluorescent Dyes
  • NS3 protein, hepatitis C virus
  • Viral Nonstructural Proteins
  • DNA Helicases