Identification of Potential HCV Inhibitors Based on the Interaction of Epigallocatechin-3-Gallate with Viral Envelope Proteins

Molecules. 2021 Feb 26;26(5):1257. doi: 10.3390/molecules26051257.

Abstract

Hepatitis C is affecting millions of people around the globe annually, which leads to death in very high numbers. After many years of research, hepatitis C virus (HCV) remains a serious threat to the human population and needs proper management. The in silico approach in the drug discovery process is an efficient method in identifying inhibitors for various diseases. In our study, the interaction between Epigallocatechin-3-gallate, a component of green tea, and envelope glycoprotein E2 of HCV is evaluated. Epigallocatechin-3-gallate is the most promising polyphenol approved through cell culture analysis that can inhibit the entry of HCV. Therefore, various in silico techniques have been employed to find out other potential inhibitors that can behave as EGCG. Thus, the homology modelling of E2 protein was performed. The potential lead molecules were predicted using ligand-based as well as structure-based virtual screening methods. The compounds obtained were then screened through PyRx. The drugs obtained were ranked based on their binding affinities. Furthermore, the docking of the topmost drugs was performed by AutoDock Vina, while its 2D interactions were plotted in LigPlot+. The lead compound mms02387687 (2-[[5-[(4-ethylphenoxy) methyl]-4-prop-2-enyl-1,2,4-triazol-3-yl] sulfanyl]-N-[3(trifluoromethyl) phenyl] acetamide) was ranked on top, and we believe it can serve as a drug against HCV in the future, owing to experimental validation.

Keywords: E2 protein; epigallocatechin-3-gallate; hepatitis C virus; homology modeling; virtual screening.

MeSH terms

  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology
  • Catechin / analogs & derivatives*
  • Catechin / chemistry
  • Catechin / pharmacology
  • Hepacivirus / drug effects*
  • Hepacivirus / genetics
  • Hepacivirus / pathogenicity
  • Hepatitis C / drug therapy*
  • Hepatitis C / virology
  • Humans
  • Ligands
  • Molecular Docking Simulation
  • Polyphenols / chemistry
  • Polyphenols / pharmacology
  • Tea / chemistry
  • Viral Envelope / chemistry
  • Viral Envelope Proteins / antagonists & inhibitors
  • Viral Envelope Proteins / genetics*
  • Virus Internalization / drug effects

Substances

  • Antiviral Agents
  • Ligands
  • Polyphenols
  • Tea
  • Viral Envelope Proteins
  • Catechin
  • epigallocatechin gallate