组装新冠肺炎免疫原性蛋白质的最抗原肽和分子佐剂开发新型多表位疫苗:生物信息学研究

N. Shams, N. Nazifi, A. Forouharmehr, A. Jaydari, Ehsan Rashidian
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引用次数: 0

摘要

它具有-0.210的重力和36.39的不稳定性指数,使它在理论上稳定。所设计的构建体被预测为可溶的和非致敏的。所提出的结构在哺乳动物网织红细胞中的半衰期约为30小时,在大肠杆菌中的半衰期超过10小时。在其三级结构中,93%的残基位于核心区,3D验证得分为52.73,Z得分为-5.55。HBHA和TLR4/MD2受体的蛋白质-蛋白质对接成功,最低能量为-130.6 kcal/mol。结论:生物信息学评价表明,所设计的结构稳定,具有免疫原性,可用于开发基于蛋白的新冠肺炎亚单位疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assembling the Most Antigenic Peptides of COVID-19 Immunogenic Proteins Along with a Molecular Adjuvant to Develop a Novel Polyepitope Vaccine: a Bioinformatics Investigation
The had -0.210 GRAVY and 36.39 instability indices which make it theoretically stable. The designed construct was predicted to be soluble and non-allergenic. The approximate half-life of the proposed structure was computed 30 hours in mammalian reticulocytes and more than 10 hours in Escherichia coli . In its tertiary structure, 93% of the residues were in the core region and had a score of 52.73 for 3D verification and -5.55 for Z-score. Protein-protein docking of HBHA and TLR4/MD2 receptor was successful with the lowest energy of -1310.6 kcal/mol. Conclusion: The bioinformatics evaluations indicate that the designed structure is stable and immunogenic for development of a protein-based subunit vaccine against COVID-19.
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