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An all-out assault on SARS-CoV-2 replication

The coronavirus pandemic has had a huge impact on public health with over 165 million people infected, 3.4 million deaths and a hugely deleterious effect on most economies. While vaccination effectively protects against the disease it is likely that viruses will evolve that can replicate in hosts im...

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Detalles Bibliográficos
Autor principal: Hay, Ronald T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286832/
https://www.ncbi.nlm.nih.gov/pubmed/34198321
http://dx.doi.org/10.1042/BCJ20210256
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author Hay, Ronald T.
author_facet Hay, Ronald T.
author_sort Hay, Ronald T.
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description The coronavirus pandemic has had a huge impact on public health with over 165 million people infected, 3.4 million deaths and a hugely deleterious effect on most economies. While vaccination effectively protects against the disease it is likely that viruses will evolve that can replicate in hosts immunised with the present vaccines. Thus, there is a great unmet need for effective antivirals that can block the development of serious disease in infected patients. The seven papers published in this issue of the Biochemical Journal address this need by expressing and purifying components required for viral replication, developing biochemical assays for these components and using the assays to screen a library of pre-existing pharmaceuticals for drugs that inhibited the target in vitro and inhibited viral replication in cell culture. The candidate drugs obtained are potential antivirals that may protect against SARS-CoV-2 infection. While not all the antiviral candidates will make it through to the clinic, they will be useful tool compounds and can act as the starting point for further drug discovery programmes.
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spelling pubmed-82868322021-08-02 An all-out assault on SARS-CoV-2 replication Hay, Ronald T. Biochem J Virology The coronavirus pandemic has had a huge impact on public health with over 165 million people infected, 3.4 million deaths and a hugely deleterious effect on most economies. While vaccination effectively protects against the disease it is likely that viruses will evolve that can replicate in hosts immunised with the present vaccines. Thus, there is a great unmet need for effective antivirals that can block the development of serious disease in infected patients. The seven papers published in this issue of the Biochemical Journal address this need by expressing and purifying components required for viral replication, developing biochemical assays for these components and using the assays to screen a library of pre-existing pharmaceuticals for drugs that inhibited the target in vitro and inhibited viral replication in cell culture. The candidate drugs obtained are potential antivirals that may protect against SARS-CoV-2 infection. While not all the antiviral candidates will make it through to the clinic, they will be useful tool compounds and can act as the starting point for further drug discovery programmes. Portland Press Ltd. 2021-07-16 2021-07-02 /pmc/articles/PMC8286832/ /pubmed/34198321 http://dx.doi.org/10.1042/BCJ20210256 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Virology
Hay, Ronald T.
An all-out assault on SARS-CoV-2 replication
title An all-out assault on SARS-CoV-2 replication
title_full An all-out assault on SARS-CoV-2 replication
title_fullStr An all-out assault on SARS-CoV-2 replication
title_full_unstemmed An all-out assault on SARS-CoV-2 replication
title_short An all-out assault on SARS-CoV-2 replication
title_sort all-out assault on sars-cov-2 replication
topic Virology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8286832/
https://www.ncbi.nlm.nih.gov/pubmed/34198321
http://dx.doi.org/10.1042/BCJ20210256
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