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An outlook on potential protein targets of COVID-19 as a druggable site
BACKGROUND: SARS-CoV-2 which causes COVID-19 disease has started a pandemic episode all over the world infecting millions of people and has created medical and economic crisis. From December 2019, cases originated from Wuhan city and started spreading at an alarming rate and has claimed millions of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256362/ https://www.ncbi.nlm.nih.gov/pubmed/35790657 http://dx.doi.org/10.1007/s11033-022-07724-3 |
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author | Noori, Rubia Sardar, Meryam |
author_facet | Noori, Rubia Sardar, Meryam |
author_sort | Noori, Rubia |
collection | PubMed |
description | BACKGROUND: SARS-CoV-2 which causes COVID-19 disease has started a pandemic episode all over the world infecting millions of people and has created medical and economic crisis. From December 2019, cases originated from Wuhan city and started spreading at an alarming rate and has claimed millions of lives till now. Scientific studies suggested that this virus showed genomic similarity of about 90% with SARS-CoV and is found to be more contagious as compared to SARS-CoV and MERS-CoV. Since the pandemic, virus has undergone constant mutation and few strains have raised public concern like Delta and Omicron variants of SARS-CoV-2. OBJECTIVE: This review focuses on the structural features of SARS-CoV-2 proteins and host proteins as well as their mechanism of action. We have also elucidated the repurposed drugs that have shown potency to inhibit these protein targets in combating COVID-19. Moreover, the article discusses the vaccines approved so far and those under clinical trials for their efficacy against COVID-19. CONCLUSION: Using cryo-electron microscopy or X-ray diffraction, hundreds of crystallographic data of SARS-CoV-2 proteins have been published including structural and non-structural proteins. These proteins have a significant role at different aspects in the viral machinery and presented themselves as potential target for drug designing and therapeutic interventions. Also, there are few host cell proteins which helps in SARS-CoV-2 entry and proteolytic cleavage required for viral infection. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9256362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-92563622022-07-06 An outlook on potential protein targets of COVID-19 as a druggable site Noori, Rubia Sardar, Meryam Mol Biol Rep Review BACKGROUND: SARS-CoV-2 which causes COVID-19 disease has started a pandemic episode all over the world infecting millions of people and has created medical and economic crisis. From December 2019, cases originated from Wuhan city and started spreading at an alarming rate and has claimed millions of lives till now. Scientific studies suggested that this virus showed genomic similarity of about 90% with SARS-CoV and is found to be more contagious as compared to SARS-CoV and MERS-CoV. Since the pandemic, virus has undergone constant mutation and few strains have raised public concern like Delta and Omicron variants of SARS-CoV-2. OBJECTIVE: This review focuses on the structural features of SARS-CoV-2 proteins and host proteins as well as their mechanism of action. We have also elucidated the repurposed drugs that have shown potency to inhibit these protein targets in combating COVID-19. Moreover, the article discusses the vaccines approved so far and those under clinical trials for their efficacy against COVID-19. CONCLUSION: Using cryo-electron microscopy or X-ray diffraction, hundreds of crystallographic data of SARS-CoV-2 proteins have been published including structural and non-structural proteins. These proteins have a significant role at different aspects in the viral machinery and presented themselves as potential target for drug designing and therapeutic interventions. Also, there are few host cell proteins which helps in SARS-CoV-2 entry and proteolytic cleavage required for viral infection. GRAPHICAL ABSTRACT: [Image: see text] Springer Netherlands 2022-07-06 2022 /pmc/articles/PMC9256362/ /pubmed/35790657 http://dx.doi.org/10.1007/s11033-022-07724-3 Text en © The Author(s), under exclusive licence to Springer Nature B.V. 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Noori, Rubia Sardar, Meryam An outlook on potential protein targets of COVID-19 as a druggable site |
title | An outlook on potential protein targets of COVID-19 as a druggable site |
title_full | An outlook on potential protein targets of COVID-19 as a druggable site |
title_fullStr | An outlook on potential protein targets of COVID-19 as a druggable site |
title_full_unstemmed | An outlook on potential protein targets of COVID-19 as a druggable site |
title_short | An outlook on potential protein targets of COVID-19 as a druggable site |
title_sort | outlook on potential protein targets of covid-19 as a druggable site |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256362/ https://www.ncbi.nlm.nih.gov/pubmed/35790657 http://dx.doi.org/10.1007/s11033-022-07724-3 |
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