Strategies for Vaccine Design for Coronavirus All Variants of Concern Using Immunoinformatics Techniques

Q4 Medicine
Anamika Basu
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Abstract

Aims: A short sequence of viral protein/ peptide could be used as a potential vaccine to treat coronavirus. Considering all variants of concern (VOC), designing a peptide vaccine for severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is a challenging task for scientists. Materials & Methods: In this study, an epitope-containing vaccine peptide in nonstructural protein 4 (nsp4) of SARS-CoV-2 was predicted. Using a modified method for both B and T cell epitope prediction (verified by molecular docking studies), linear B and T cell epitopes of nsp4 protein were predicted. Predicted epitopes were analyzed with population coverage calculation and epitope conservancy analysis. Findings: The short peptide sequence74QRGGSYTNDKA84 was selected as B-cell epitope by considering the scores of surface accessibility, hydrophilicity, and beta turn for each amino acid residue. Similarly, the peptide sequences 359 FLAHIQWMV367 and359FLAHIQWVMFTPLV373 were predicted as T cell epitopes for MHC-I and MHC-II molecules. These two potential epitopes could favor HLA-A*02:01 and HLA-DRB*01:01 as MHC allelic proteins with the lowest IC50 values, respectively. No amino acid mutations were observed in GISAID (global initiative on sharing all influenza data) database for alpha, beta, gamma, and delta variants of concerns. Among seven amino acid point mutations in nsp4 protein of omicron variant, none were present in the peptide sequences of the predicted epitopes. Conclusion: Short peptide sequences could be predicted as vaccines to prevent infections caused by coronavirus variants of concerns. © 2022, TMU Press.
利用免疫信息学技术设计冠状病毒所有变体疫苗的策略
目的:病毒蛋白/肽短序列可作为治疗冠状病毒的潜在疫苗。考虑到所有关注的变异(VOC),设计一种针对严重急性呼吸综合征冠状病毒2 (SARS CoV-2)的肽疫苗对科学家来说是一项具有挑战性的任务。材料与方法:本研究预测了SARS-CoV-2非结构蛋白4 (nsp4)中含有表位的疫苗肽。采用改进的B和T细胞表位预测方法(通过分子对接研究验证),预测了nsp4蛋白的线性B和T细胞表位。对预测表位进行种群覆盖率计算和表位保护分析。结果:通过对每个氨基酸残基的表面可及性、亲水性和β转数评分,选择短肽序列74qrggsytndka84作为b细胞表位。同样,预测肽序列359 FLAHIQWMV367和359flahiqwvmftplv373作为MHC-I和MHC-II分子的T细胞表位。这两个潜在表位分别有利于HLA-A*02:01和HLA-DRB*01:01作为最低IC50值的MHC等位蛋白。在GISAID(全球共享所有流感数据倡议)数据库中未观察到有关α、β、γ和δ变异的氨基酸突变。在组粒变异nsp4蛋白的7个氨基酸点突变中,预测表位的肽序列中没有出现突变。结论:预测短肽序列可作为预防冠状病毒变异引起的感染的疫苗。©2022,TMU出版社。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.50
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0.00%
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20
审稿时长
6 weeks
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