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Rapid resistance profiling of SARS-CoV-2 protease inhibitors
Resistance to nirmatrelvir (Paxlovid) has been shown by multiple groups and may already exist in clinical SARS-CoV-2 isolates. Here a panel of SARS-CoV-2 main protease (M(pro)) variants and a robust cell-based assay are used to compare the resistance profiles of nirmatrelvir, ensitrelvir, and FB2001...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002627/ https://www.ncbi.nlm.nih.gov/pubmed/36909573 http://dx.doi.org/10.1101/2023.02.25.530000 |
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author | Moghadasi, Seyed Arad Biswas, Rayhan G. Harki, Daniel A. Harris, Reuben S. |
author_facet | Moghadasi, Seyed Arad Biswas, Rayhan G. Harki, Daniel A. Harris, Reuben S. |
author_sort | Moghadasi, Seyed Arad |
collection | PubMed |
description | Resistance to nirmatrelvir (Paxlovid) has been shown by multiple groups and may already exist in clinical SARS-CoV-2 isolates. Here a panel of SARS-CoV-2 main protease (M(pro)) variants and a robust cell-based assay are used to compare the resistance profiles of nirmatrelvir, ensitrelvir, and FB2001. The results reveal distinct resistance mechanisms (“fingerprints”) and indicate that these next-generation drugs have the potential to be effective against nirmatrelvir-resistant variants and vice versa. |
format | Online Article Text |
id | pubmed-10002627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100026272023-03-11 Rapid resistance profiling of SARS-CoV-2 protease inhibitors Moghadasi, Seyed Arad Biswas, Rayhan G. Harki, Daniel A. Harris, Reuben S. bioRxiv Article Resistance to nirmatrelvir (Paxlovid) has been shown by multiple groups and may already exist in clinical SARS-CoV-2 isolates. Here a panel of SARS-CoV-2 main protease (M(pro)) variants and a robust cell-based assay are used to compare the resistance profiles of nirmatrelvir, ensitrelvir, and FB2001. The results reveal distinct resistance mechanisms (“fingerprints”) and indicate that these next-generation drugs have the potential to be effective against nirmatrelvir-resistant variants and vice versa. Cold Spring Harbor Laboratory 2023-02-27 /pmc/articles/PMC10002627/ /pubmed/36909573 http://dx.doi.org/10.1101/2023.02.25.530000 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Moghadasi, Seyed Arad Biswas, Rayhan G. Harki, Daniel A. Harris, Reuben S. Rapid resistance profiling of SARS-CoV-2 protease inhibitors |
title | Rapid resistance profiling of SARS-CoV-2 protease inhibitors |
title_full | Rapid resistance profiling of SARS-CoV-2 protease inhibitors |
title_fullStr | Rapid resistance profiling of SARS-CoV-2 protease inhibitors |
title_full_unstemmed | Rapid resistance profiling of SARS-CoV-2 protease inhibitors |
title_short | Rapid resistance profiling of SARS-CoV-2 protease inhibitors |
title_sort | rapid resistance profiling of sars-cov-2 protease inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002627/ https://www.ncbi.nlm.nih.gov/pubmed/36909573 http://dx.doi.org/10.1101/2023.02.25.530000 |
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