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Recent insights into the structure and function of coronavirus ribonucleases
Coronaviruses use approximately two‐thirds of their 30‐kb genomes to encode nonstructural proteins (nsps) with diverse functions that assist in viral replication and transcription, and evasion of the host immune response. The SARS‐CoV‐2 pandemic has led to renewed interest in the molecular mechanism...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110870/ https://www.ncbi.nlm.nih.gov/pubmed/35445579 http://dx.doi.org/10.1002/2211-5463.13414 |
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author | Frazier, Meredith N. Riccio, Amanda A. Wilson, Isha M. Copeland, William C. Stanley, Robin E. |
author_facet | Frazier, Meredith N. Riccio, Amanda A. Wilson, Isha M. Copeland, William C. Stanley, Robin E. |
author_sort | Frazier, Meredith N. |
collection | PubMed |
description | Coronaviruses use approximately two‐thirds of their 30‐kb genomes to encode nonstructural proteins (nsps) with diverse functions that assist in viral replication and transcription, and evasion of the host immune response. The SARS‐CoV‐2 pandemic has led to renewed interest in the molecular mechanisms used by coronaviruses to infect cells and replicate. Among the 16 Nsps involved in replication and transcription, coronaviruses encode two ribonucleases that process the viral RNA—an exonuclease (Nsp14) and an endonuclease (Nsp15). In this review, we discuss recent structural and biochemical studies of these nucleases and the implications for drug discovery. |
format | Online Article Text |
id | pubmed-9110870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91108702022-05-17 Recent insights into the structure and function of coronavirus ribonucleases Frazier, Meredith N. Riccio, Amanda A. Wilson, Isha M. Copeland, William C. Stanley, Robin E. FEBS Open Bio Reviews Coronaviruses use approximately two‐thirds of their 30‐kb genomes to encode nonstructural proteins (nsps) with diverse functions that assist in viral replication and transcription, and evasion of the host immune response. The SARS‐CoV‐2 pandemic has led to renewed interest in the molecular mechanisms used by coronaviruses to infect cells and replicate. Among the 16 Nsps involved in replication and transcription, coronaviruses encode two ribonucleases that process the viral RNA—an exonuclease (Nsp14) and an endonuclease (Nsp15). In this review, we discuss recent structural and biochemical studies of these nucleases and the implications for drug discovery. John Wiley and Sons Inc. 2022-04-29 /pmc/articles/PMC9110870/ /pubmed/35445579 http://dx.doi.org/10.1002/2211-5463.13414 Text en © 2022 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Frazier, Meredith N. Riccio, Amanda A. Wilson, Isha M. Copeland, William C. Stanley, Robin E. Recent insights into the structure and function of coronavirus ribonucleases |
title | Recent insights into the structure and function of coronavirus ribonucleases |
title_full | Recent insights into the structure and function of coronavirus ribonucleases |
title_fullStr | Recent insights into the structure and function of coronavirus ribonucleases |
title_full_unstemmed | Recent insights into the structure and function of coronavirus ribonucleases |
title_short | Recent insights into the structure and function of coronavirus ribonucleases |
title_sort | recent insights into the structure and function of coronavirus ribonucleases |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110870/ https://www.ncbi.nlm.nih.gov/pubmed/35445579 http://dx.doi.org/10.1002/2211-5463.13414 |
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