Detecting SARS-CoV-2 3CLpro expression and activity using a polyclonal antiserum and a luciferase-based biosensor

Virology. 2021 Apr:556:73-78. doi: 10.1016/j.virol.2021.01.010. Epub 2021 Jan 26.

Abstract

The need to stem the current outbreak of SARS-CoV-2 responsible for COVID-19 is driving the search for inhibitors that will block coronavirus replication and pathogenesis. The coronavirus 3C-like protease (3CLpro) encoded in the replicase polyprotein is an attractive target for antiviral drug development because protease activity is required for generating a functional replication complex. Reagents that can be used to screen for protease inhibitors and for identifying the replicase products of SARS-CoV-2 are urgently needed. Here we describe a luminescence-based biosensor assay for evaluating small molecule inhibitors of SARS-CoV-2 3CLpro/main protease. We also document that a polyclonal rabbit antiserum developed against SARS-CoV 3CLpro cross reacts with the highly conserved 3CLpro of SARS-CoV-2. These reagents will facilitate the pre-clinical evaluation of SARS-CoV-2 protease inhibitors.

Keywords: 3CLpro; Main protease; Mpro; Protease inhibitors; SARS-CoV-2; nsp5; pGlo biosensor.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Biosensing Techniques / methods*
  • Coronavirus 3C Proteases / antagonists & inhibitors
  • Coronavirus 3C Proteases / genetics
  • Coronavirus 3C Proteases / immunology
  • Coronavirus 3C Proteases / metabolism*
  • Cross Reactions
  • Immune Sera / immunology*
  • Luciferases / genetics
  • Luciferases / metabolism*
  • Protease Inhibitors / pharmacology
  • Rabbits
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • SARS-CoV-2 / drug effects
  • SARS-CoV-2 / genetics
  • SARS-CoV-2 / immunology
  • SARS-CoV-2 / metabolism*
  • Severe acute respiratory syndrome-related coronavirus / immunology
  • Severe acute respiratory syndrome-related coronavirus / metabolism
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / immunology
  • Viral Nonstructural Proteins / metabolism
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Immune Sera
  • Protease Inhibitors
  • Recombinant Fusion Proteins
  • Viral Nonstructural Proteins
  • Luciferases
  • 3C-like proteinase, SARS-CoV-2
  • Coronavirus 3C Proteases