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Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein
The far-reaching effects of the SARS-CoV-2 pandemic have crippled the progress of the world today. With the introduction of newer and newer mutated variants of the virus, it has become necessary to have a vaccine that remains useful against all the mutated strains of SARS-CoV-2. In this regard, pept...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863349/ https://www.ncbi.nlm.nih.gov/pubmed/35221449 http://dx.doi.org/10.1016/j.mehy.2022.110810 |
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author | Biswas, Subhamoy Dey, Sumanta Chatterjee, Shreyans Nandy, Ashesh |
author_facet | Biswas, Subhamoy Dey, Sumanta Chatterjee, Shreyans Nandy, Ashesh |
author_sort | Biswas, Subhamoy |
collection | PubMed |
description | The far-reaching effects of the SARS-CoV-2 pandemic have crippled the progress of the world today. With the introduction of newer and newer mutated variants of the virus, it has become necessary to have a vaccine that remains useful against all the mutated strains of SARS-CoV-2. In this regard, peptide vaccines turn out to be a cheap alternative to the traditionally designed vaccines owing to their much quicker and computationally easier, and more robust design procedures. Here, in this article, we hypothesize that there are three possible peptide vaccine regions that can be targeted to prevent the surge of SARS-CoV-2. The candidates that were selected, were surface-exposed and were not sequestered by any neighbouring amino acids. They were also found to be capable of generating both B-cell and T-cell immune responses. Most importantly, none of them contains any spike protein mutation of the currently prevailing variants of SARS-CoV-2. From these findings, we have therefore concluded that these three regions can be used in wet labs for peptide vaccine design against the upcoming strains of SARS-CoV-2. |
format | Online Article Text |
id | pubmed-8863349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88633492022-02-23 Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein Biswas, Subhamoy Dey, Sumanta Chatterjee, Shreyans Nandy, Ashesh Med Hypotheses Article The far-reaching effects of the SARS-CoV-2 pandemic have crippled the progress of the world today. With the introduction of newer and newer mutated variants of the virus, it has become necessary to have a vaccine that remains useful against all the mutated strains of SARS-CoV-2. In this regard, peptide vaccines turn out to be a cheap alternative to the traditionally designed vaccines owing to their much quicker and computationally easier, and more robust design procedures. Here, in this article, we hypothesize that there are three possible peptide vaccine regions that can be targeted to prevent the surge of SARS-CoV-2. The candidates that were selected, were surface-exposed and were not sequestered by any neighbouring amino acids. They were also found to be capable of generating both B-cell and T-cell immune responses. Most importantly, none of them contains any spike protein mutation of the currently prevailing variants of SARS-CoV-2. From these findings, we have therefore concluded that these three regions can be used in wet labs for peptide vaccine design against the upcoming strains of SARS-CoV-2. Elsevier Ltd. 2022-04 2022-02-22 /pmc/articles/PMC8863349/ /pubmed/35221449 http://dx.doi.org/10.1016/j.mehy.2022.110810 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Biswas, Subhamoy Dey, Sumanta Chatterjee, Shreyans Nandy, Ashesh Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein |
title | Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein |
title_full | Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein |
title_fullStr | Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein |
title_full_unstemmed | Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein |
title_short | Combatting future variants of SARS-CoV-2 using an in-silico peptide vaccine approach by targeting the spike protein |
title_sort | combatting future variants of sars-cov-2 using an in-silico peptide vaccine approach by targeting the spike protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863349/ https://www.ncbi.nlm.nih.gov/pubmed/35221449 http://dx.doi.org/10.1016/j.mehy.2022.110810 |
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