Reversible covalent inhibitors suppress enterovirus 71 infection by targeting the 3C protease

Antiviral Res. 2021 Aug:192:105102. doi: 10.1016/j.antiviral.2021.105102. Epub 2021 Jun 1.

Abstract

As one of the principal etiological agents of hand, foot, and mouth disease (HFMD), enterovirus 71 (EV71) is associated with severe neurological complications or fatal diseases, while without effective medications thus far. Here we applied dually activated Michael acceptor to develop a series of reversible covalent compounds for EV71 3C protease (3Cpro), a promising antiviral drug target that plays an essential role during viral replication by cleaving the precursor polyprotein, inhibiting host protein synthesis, and evading innate immunity. Among them, cyanoacrylate and Boc-protected cyanoarylamide derivatives (SLQ-4 and SLQ-5) showed effective antiviral activity against EV71. The two inhibitors exhibited broad antiviral effects, acting on RD, 293T, and Vero cell lines, as well as on EV71 A, B, C, CVA16, and CVB3 viral strains. We further determined the binding pockets between the two inhibitors and 3Cpro based on docking studies. These results, together with our previous studies, provide evidence to elucidate the mechanism of action of these two reversible covalent inhibitors and contribute to the development of clinically effective medicines to treat EV71 infections.

Keywords: EV71; Protease; Reversible covalent inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3C Viral Proteases / antagonists & inhibitors*
  • 3C Viral Proteases / chemistry
  • Acrylamides / chemistry
  • Acrylamides / pharmacology
  • Animals
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Cell Line
  • Cell Survival / drug effects
  • Cyanoacrylates / chemistry
  • Cyanoacrylates / pharmacology
  • Enterovirus / classification
  • Enterovirus / drug effects
  • Enterovirus A, Human / drug effects*
  • Enterovirus Infections / virology
  • Humans
  • Molecular Docking Simulation
  • Protease Inhibitors / chemistry
  • Protease Inhibitors / pharmacology*
  • Virus Replication / drug effects

Substances

  • Acrylamides
  • Antiviral Agents
  • Cyanoacrylates
  • Protease Inhibitors
  • 3C Viral Proteases