De novo design of anti-variant COVID-19 vaccine.

IF 2.5 Q3 BIOCHEMICAL RESEARCH METHODS Biology Methods and Protocols Pub Date : 2023-09-26 eCollection Date: 2023-01-01 DOI:10.1093/biomethods/bpad021
Arpita Goswami, Madan Kumar, Samee Ullah, Milind M Gore
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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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抗变异新冠肺炎疫苗的从头设计。
最近的研究强调了结合野生型核衣壳和刺突蛋白的严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)混合疫苗的有效性。我们通过整合德尔塔和奥密克戎变体的刺突蛋白突变,进一步加强了这一策略。德尔塔和奥密克戎都标志着未接种疫苗和接种疫苗患者的病毒传播性和严重程度的变化。因此,它们的突变对未来的病毒变异也至关重要。奥密克戎特别擅长通过突变刺突表位来逃避免疫。奥密克戎和亚变种对基于刺突的疫苗的快速适应以及同时的传播性,突显了新疫苗在持续抗击严重急性呼吸系统综合征冠状病毒2型中的紧迫性。因此,我们添加了三种持久的T细胞刺激核衣壳肽,类似于季节性人类冠状病毒(HuCoV)的同源序列,以及一种引发强烈T细胞免疫反应的包膜肽。这些肽与非免疫原性连接体聚集在杂交刺突的细胞质区域,从而实现系统排列。AlphaFold(基于人工智能的模型构建)分析表明,省略跨膜结构域可以提高这些细胞质表位的折叠效率,从而确保CD4+结构表位的持久免疫。进一步的分子动力学模拟验证了模型结构的紧凑构象和柔性C末端区域。总体而言,在整个模拟过程中,结构显示出稳定性和较小的构象波动。此外,AlphaFold预测的结构表位在模拟过程中保持折叠,以确保接种疫苗后CD4+T细胞反应的特异性。我们提出的方法可以提供将类似于HuCoV的多种抗病毒T细胞肽掺入连接区的选择。这种多功能性有望解决各种病毒的爆发和挑战,以便在这个创新疫苗时代进行有效管理。
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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来源期刊
Biology Methods and Protocols
Biology Methods and Protocols Agricultural and Biological Sciences-Agricultural and Biological Sciences (all)
CiteScore
3.80
自引率
2.80%
发文量
28
审稿时长
19 weeks
期刊最新文献
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