Cited by 2vaccines and immunoinformatics approachesSARS-CoV-2 and COVID-19 ResearchProtein Structure and Dynamics

De novo design of anti-variant COVID-19 vaccine

Open access
Goswami, Arpita, Kumar, Madan, Ullah, Samee, Gore, Milind M·2023·Biology Methods and Protocols

Published version of a preprint

Abstract

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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Authors
Goswami, A., Kumar, M., Ullah, S., & Gore, M. M.
Affiliations
  • Kshamalab, Leo’s Research Services and Suppliers , Mysuru 570016, India
  • Uppsala University (SE)
  • National Center for Bioinformatics (NCB) , Islamabad 45320, Pakistan
  • 5/1B, Krutika Co-Op Housing Society , Kothrud, Pune 411039, India
Corresponding author
Goswami, Arpita
Venue
Biology Methods and Protocols
Published
2023-01-01
Volume
8
Issue
1
Pages
bpad021-bpad021
ISSN
2396-8923 (ISSN-L)
OpenAlex
W4387081101
Cited by
2
References
6
Citations by year
2025: 2
FWCI
0.18
Type
journal article
Language
en
Open access
Locations
  • Biology Methods and Protocols (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Uppsala University Publications (Uppsala University) (submittedVersion, other-oa)
Funders
  • Vetenskapsrådet (05973, 2018-, 201805973, 2022-06725, No. 2018-05973)
  • Uppsala Multidisciplinary Center for Advanced Computational Science
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
  • Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
Keywords
COVID-19 vaccine design, SARS-CoV-2, nucleocapsid protein, spike protein mutations, Omicron variant, Delta variant, T cell epitopes, CD4+ T cell responses, transmembrane domain deletion, vaccine stability, molecular dynamics simulation, AlphaFold structure prediction

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