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Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins

More than one and half years have passed, as of August 2021, since the COVID-19 caused by the novel coronavirus named SARS-CoV-2 emerged in 2019. While the recent success of vaccine developments likely reduces the severe cases, there is still a strong requirement of safety and effective therapeutic...

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Autores principales: Hijikata, Atsushi, Shionyu, Clara, Nakae, Setsu, Shionyu, Masafumi, Ota, Motonori, Kanaya, Shigehiko, Shirai, Tsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society of Japan 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550875/
https://www.ncbi.nlm.nih.gov/pubmed/34745807
http://dx.doi.org/10.2142/biophysico.bppb-v18.025
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author Hijikata, Atsushi
Shionyu, Clara
Nakae, Setsu
Shionyu, Masafumi
Ota, Motonori
Kanaya, Shigehiko
Shirai, Tsuyoshi
author_facet Hijikata, Atsushi
Shionyu, Clara
Nakae, Setsu
Shionyu, Masafumi
Ota, Motonori
Kanaya, Shigehiko
Shirai, Tsuyoshi
author_sort Hijikata, Atsushi
collection PubMed
description More than one and half years have passed, as of August 2021, since the COVID-19 caused by the novel coronavirus named SARS-CoV-2 emerged in 2019. While the recent success of vaccine developments likely reduces the severe cases, there is still a strong requirement of safety and effective therapeutic drugs for overcoming the unprecedented situation. Here we review the recent progress and the status of the drug discovery against COVID-19 with emphasizing a structure-based perspective. Structural data regarding the SARS-CoV-2 proteome has been rapidly accumulated in the Protein Data Bank, and up to 68% of the total amino acid residues encoded in the genome were covered by the structural data. Despite a global effort of in silico and in vitro screenings for drug repurposing, there is only a limited number of drugs had been successfully authorized by drug regulation organizations. Although many approved drugs and natural compounds, which exhibited antiviral activity in vitro, were considered potential drugs against COVID-19, a further multidisciplinary investigation is required for understanding the mechanisms underlying the antiviral effects of the drugs.
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spelling pubmed-85508752021-11-05 Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins Hijikata, Atsushi Shionyu, Clara Nakae, Setsu Shionyu, Masafumi Ota, Motonori Kanaya, Shigehiko Shirai, Tsuyoshi Biophys Physicobiol Review Article More than one and half years have passed, as of August 2021, since the COVID-19 caused by the novel coronavirus named SARS-CoV-2 emerged in 2019. While the recent success of vaccine developments likely reduces the severe cases, there is still a strong requirement of safety and effective therapeutic drugs for overcoming the unprecedented situation. Here we review the recent progress and the status of the drug discovery against COVID-19 with emphasizing a structure-based perspective. Structural data regarding the SARS-CoV-2 proteome has been rapidly accumulated in the Protein Data Bank, and up to 68% of the total amino acid residues encoded in the genome were covered by the structural data. Despite a global effort of in silico and in vitro screenings for drug repurposing, there is only a limited number of drugs had been successfully authorized by drug regulation organizations. Although many approved drugs and natural compounds, which exhibited antiviral activity in vitro, were considered potential drugs against COVID-19, a further multidisciplinary investigation is required for understanding the mechanisms underlying the antiviral effects of the drugs. The Biophysical Society of Japan 2021-10-05 /pmc/articles/PMC8550875/ /pubmed/34745807 http://dx.doi.org/10.2142/biophysico.bppb-v18.025 Text en 2021 THE BIOPHYSICAL SOCIETY OF JAPAN https://creativecommons.org/licenses/by-nc-sa/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 Inter­national License. To view a copy of this license, visit 
https://creativecommons.org/licenses/by-nc-sa/4.0/.
spellingShingle Review Article
Hijikata, Atsushi
Shionyu, Clara
Nakae, Setsu
Shionyu, Masafumi
Ota, Motonori
Kanaya, Shigehiko
Shirai, Tsuyoshi
Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins
title Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins
title_full Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins
title_fullStr Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins
title_full_unstemmed Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins
title_short Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins
title_sort current status of structure-based drug repurposing against covid-19 by targeting sars-cov-2 proteins
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8550875/
https://www.ncbi.nlm.nih.gov/pubmed/34745807
http://dx.doi.org/10.2142/biophysico.bppb-v18.025
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