Molecular dynamics simulation revealed binding of nucleotide inhibitors to ZIKV polymerase over 444 nanoseconds

J Med Virol. 2018 Jan;90(1):13-18. doi: 10.1002/jmv.24934. Epub 2017 Sep 18.

Abstract

In the year 2015, new Zika virus (ZIKV) broke out in Brazil and spread away in more than 80 countries. Scientists directed their efforts toward viral polymerase in attempt to find inhibitors that might interfere with its function. In this study, molecular dynamics simulation (MDS) was performed over 444 ns for a ZIKV polymerase model. Molecular docking (MD) was then performed every 10 ns during the MDS course to ensure the binding of small molecules to the polymerase over the entire time of the simulation. MD revealed the binding ability of four suggested guanosine inhibitors (GIs); (Guanosine substituted with OH and SH (phenyl) oxidanyl in the 2' carbon of the ribose ring). The GIs were compared to guanosine triphosphate (GTP) and five anti-hepatitis C virus drugs (either approved or under clinical trials). The mode of binding and the binding performance of GIs to ZIKV polymerase were found to be the same as GTP. Hence, these compounds were capable of competing GTP for the active site. Moreover, GIs bound to ZIKV active site more tightly compared to ribavirin, the wide-range antiviral drug.

Keywords: Zika virus; guanosine inhibitors; molecular docking; molecular dynamics simulation; polymerase; protein-ligand docking.

MeSH terms

  • Antiviral Agents / chemistry
  • Antiviral Agents / metabolism*
  • Antiviral Agents / pharmacology*
  • Binding Sites
  • Brazil
  • Guanosine / antagonists & inhibitors
  • Guanosine Triphosphate / analogs & derivatives
  • Guanosine Triphosphate / chemistry
  • Humans
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Nucleotides / antagonists & inhibitors*
  • RNA-Dependent RNA Polymerase / metabolism*
  • Zika Virus / drug effects*
  • Zika Virus / enzymology
  • Zika Virus / metabolism*

Substances

  • Antiviral Agents
  • Nucleotides
  • Guanosine
  • Guanosine Triphosphate
  • RNA-Dependent RNA Polymerase