Development of a colorimetric assay for the detection of SARS-CoV-2 3CLpro activity.
cam.depositDate | 2022-06-24 | |
cam.issuedOnline | 2022-04-21 | |
dc.contributor.author | Garland, Gavin D | |
dc.contributor.author | Harvey, Robert F | |
dc.contributor.author | Mulroney, Thomas E | |
dc.contributor.author | Monti, Mie | |
dc.contributor.author | Fuller, Stewart | |
dc.contributor.author | Haigh, Richard | |
dc.contributor.author | Gerber, Pehuén Pereyra | |
dc.contributor.author | Barer, Michael R | |
dc.contributor.author | Matheson, Nicholas J | |
dc.contributor.author | Willis, Anne E | |
dc.contributor.orcid | Willis, Anne E [0000-0002-1470-8531] | |
dc.date.accessioned | 2022-06-24T23:30:55Z | |
dc.date.available | 2022-06-24T23:30:55Z | |
dc.date.issued | 2022-04-29 | |
dc.date.updated | 2022-06-24T10:02:51Z | |
dc.description.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. | |
dc.format.medium | ||
dc.identifier.doi | 10.17863/CAM.85771 | |
dc.identifier.eissn | 1470-8728 | |
dc.identifier.issn | 0264-6021 | |
dc.identifier.uri | https://www.repository.cam.ac.uk/handle/1810/338362 | |
dc.language.iso | eng | |
dc.publisher | Portland Press Ltd. | |
dc.publisher.department | Department of Medicine | |
dc.publisher.department | Department of Pharmacology | |
dc.publisher.url | http://dx.doi.org/10.1042/bcj20220105 | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | COVID 19 | |
dc.subject | Coronavirus | |
dc.subject | assay development | |
dc.subject | Antiviral Agents | |
dc.subject | COVID-19 | |
dc.subject | Colorimetry | |
dc.subject | Coronavirus 3C Proteases | |
dc.subject | Gold | |
dc.subject | HEK293 Cells | |
dc.subject | Humans | |
dc.subject | Metal Nanoparticles | |
dc.subject | Peptide Hydrolases | |
dc.subject | Protease Inhibitors | |
dc.subject | SARS-CoV-2 | |
dc.title | Development of a colorimetric assay for the detection of SARS-CoV-2 3CLpro activity. | |
dc.type | Article | |
dcterms.dateAccepted | 2022-04-04 | |
prism.endingPage | 920 | |
prism.issueIdentifier | 8 | |
prism.publicationDate | 2022 | |
prism.publicationName | Biochem J | |
prism.startingPage | 901 | |
prism.volume | 479 | |
pubs.funder-project-id | Medical Research Council (MR/P008801/1) | |
pubs.licence-display-name | Apollo Repository Deposit Licence Agreement | |
pubs.licence-identifier | apollo-deposit-licence-2-1 | |
rioxxterms.type | Journal Article/Review | |
rioxxterms.version | VoR | |
rioxxterms.versionofrecord | 10.1042/BCJ20220105 |
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