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De novo design of anti-variant COVID-19 vaccine

Recent studies highlight the effectiveness of hybrid Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) vaccines combining wild-type nucleocapsid and Spike proteins. We have further enhanced this strategy by incorporating delta and omicron variants’ spike protein mutations. Both delta and...

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Autores principales: Goswami, Arpita, Kumar, Madan, Ullah, Samee, Gore, Milind M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580973/
https://www.ncbi.nlm.nih.gov/pubmed/37854896
http://dx.doi.org/10.1093/biomethods/bpad021
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author Goswami, Arpita
Kumar, Madan
Ullah, Samee
Gore, Milind M
author_facet Goswami, Arpita
Kumar, Madan
Ullah, Samee
Gore, Milind M
author_sort Goswami, Arpita
collection PubMed
description Recent studies highlight the effectiveness of hybrid Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) vaccines combining wild-type nucleocapsid and Spike proteins. We have further enhanced this strategy by incorporating delta and omicron variants’ spike protein mutations. Both delta and omicron mark the shifts in viral transmissibility and severity in unvaccinated and vaccinated patients. So their mutations are highly crucial for future viral variants also. Omicron is particularly adept at immune evasion by mutating spike epitopes. The rapid adaptations of Omicron and sub-variants to spike-based vaccines and simultaneous transmissibility underline the urgency for new vaccines in the continuous battle against SARS-CoV-2. Therefore, we have added three persistent T-cell-stimulating nucleocapsid peptides similar to homologous sequences from seasonal Human Coronaviruses (HuCoV) and an envelope peptide that elicits a strong T-cell immune response. These peptides are clustered in the hybrid spike’s cytoplasmic region with non-immunogenic linkers, enabling systematic arrangement. AlphaFold (Artificial intelligence-based model building) analysis suggests omitting the transmembrane domain enhances these cytoplasmic epitopes’ folding efficiency which can ensure persistent immunity for CD4(+) structural epitopes. Further molecular dynamics simulations validate the compact conformation of the modeled structures and a flexible C-terminus region. Overall, the structures show stability and less conformational fluctuation throughout the simulation. Also, the AlphaFold predicted structural epitopes maintained their folds during simulation to ensure the specificity of CD4(+) T-cell response after vaccination. Our proposed approach may provide options for incorporating diverse anti-viral T-cell peptides, similar to HuCoV, into linker regions. This versatility can be promising to address outbreaks and challenges posed by various viruses for effective management in this era of innovative vaccines.
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spelling pubmed-105809732023-10-18 De novo design of anti-variant COVID-19 vaccine Goswami, Arpita Kumar, Madan Ullah, Samee Gore, Milind M Biol Methods Protoc Special Collection: Covid19 Methods & Protocols Recent studies highlight the effectiveness of hybrid Severe Acute Respiratory Syndrome-Coronavirus-2 (SARS-CoV-2) vaccines combining wild-type nucleocapsid and Spike proteins. We have further enhanced this strategy by incorporating delta and omicron variants’ spike protein mutations. Both delta and omicron mark the shifts in viral transmissibility and severity in unvaccinated and vaccinated patients. So their mutations are highly crucial for future viral variants also. Omicron is particularly adept at immune evasion by mutating spike epitopes. The rapid adaptations of Omicron and sub-variants to spike-based vaccines and simultaneous transmissibility underline the urgency for new vaccines in the continuous battle against SARS-CoV-2. Therefore, we have added three persistent T-cell-stimulating nucleocapsid peptides similar to homologous sequences from seasonal Human Coronaviruses (HuCoV) and an envelope peptide that elicits a strong T-cell immune response. These peptides are clustered in the hybrid spike’s cytoplasmic region with non-immunogenic linkers, enabling systematic arrangement. AlphaFold (Artificial intelligence-based model building) analysis suggests omitting the transmembrane domain enhances these cytoplasmic epitopes’ folding efficiency which can ensure persistent immunity for CD4(+) structural epitopes. Further molecular dynamics simulations validate the compact conformation of the modeled structures and a flexible C-terminus region. Overall, the structures show stability and less conformational fluctuation throughout the simulation. Also, the AlphaFold predicted structural epitopes maintained their folds during simulation to ensure the specificity of CD4(+) T-cell response after vaccination. Our proposed approach may provide options for incorporating diverse anti-viral T-cell peptides, similar to HuCoV, into linker regions. This versatility can be promising to address outbreaks and challenges posed by various viruses for effective management in this era of innovative vaccines. Oxford University Press 2023-09-26 /pmc/articles/PMC10580973/ /pubmed/37854896 http://dx.doi.org/10.1093/biomethods/bpad021 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Collection: Covid19 Methods & Protocols
Goswami, Arpita
Kumar, Madan
Ullah, Samee
Gore, Milind M
De novo design of anti-variant COVID-19 vaccine
title De novo design of anti-variant COVID-19 vaccine
title_full De novo design of anti-variant COVID-19 vaccine
title_fullStr De novo design of anti-variant COVID-19 vaccine
title_full_unstemmed De novo design of anti-variant COVID-19 vaccine
title_short De novo design of anti-variant COVID-19 vaccine
title_sort de novo design of anti-variant covid-19 vaccine
topic Special Collection: Covid19 Methods & Protocols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580973/
https://www.ncbi.nlm.nih.gov/pubmed/37854896
http://dx.doi.org/10.1093/biomethods/bpad021
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