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Development of a colorimetric assay for the detection of SARS-CoV-2 3CLpro activity.
Garland, Gavin D; Harvey, Robert F; Mulroney, Thomas E; Monti, Mie; Fuller, Stewart; Haigh, Richard; Gerber, Pehuén Pereyra; Barer, Michael R; Matheson, Nicholas J; Willis, Anne E.
  • Garland GD; MRC Toxicology Unit, Gleeson Building, Tennis Court Rd, Cambridge, U.K.
  • Harvey RF; MRC Toxicology Unit, Gleeson Building, Tennis Court Rd, Cambridge, U.K.
  • Mulroney TE; MRC Toxicology Unit, Gleeson Building, Tennis Court Rd, Cambridge, U.K.
  • Monti M; MRC Toxicology Unit, Gleeson Building, Tennis Court Rd, Cambridge, U.K.
  • Fuller S; Department of Medicine, University of Cambridge, Cambridge, U.K.
  • Haigh R; Department of Respiratory Sciences, Maurice Shock Medical Sciences Building, University Road, Leicester, U.K.
  • Gerber PP; Department of Medicine, University of Cambridge, Cambridge, U.K.
  • Barer MR; Cambridge Institute of Therapeutic Immunology and Infectious Disease (CITIID), University of Cambridge, Cambridge, U.K.
  • Matheson NJ; Department of Respiratory Sciences, Maurice Shock Medical Sciences Building, University Road, Leicester, U.K.
  • Willis AE; Department of Medicine, University of Cambridge, Cambridge, U.K.
Biochem J ; 479(8): 901-920, 2022 04 29.
Article in English | MEDLINE | ID: covidwho-1774010
ABSTRACT
Diagnostic testing continues to be an integral component of the strategy to contain the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) global pandemic, the causative agent of Coronavirus Disease 2019 (COVID-19). The SARS-CoV-2 genome encodes the 3C-like protease (3CLpro) which is essential for coronavirus replication. This study adapts an in vitro colorimetric gold nanoparticle (AuNP) based protease assay to specifically detect the activity of SARS-CoV-2 3CLpro as a purified recombinant protein and as a cellular protein exogenously expressed in HEK293T human cells. We also demonstrate that the specific sensitivity of the assay for SARS-CoV-2 3CLpro can be improved by use of an optimised peptide substrate and through hybrid dimerisation with inactive 3CLpro mutant monomers. These findings highlight the potential for further development of the AuNP protease assay to detect SARS-CoV-2 3CLpro activity as a novel, accessible and cost-effective diagnostic test for SARS-CoV-2 infection at the point-of-care. Importantly, this versatile assay could also be easily adapted to detect specific protease activity associated with other viruses or diseases conditions.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Metal Nanoparticles / COVID-19 Type of study: Diagnostic study Limits: Humans Language: English Journal: Biochem J Year: 2022 Document Type: Article Affiliation country: Bcj20220105

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Metal Nanoparticles / COVID-19 Type of study: Diagnostic study Limits: Humans Language: English Journal: Biochem J Year: 2022 Document Type: Article Affiliation country: Bcj20220105