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Design and Antigenic Epitopes Prediction of a New Trial Recombinant Multiepitopic Rotaviral Vaccine: In Silico Analyses

机译:新的重组多表位轮状病毒疫苗的设计和抗原表位预测:计算机模拟分析。

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摘要

Rotavirus is the major etiologic factor of severe diarrheal disease. Natural infection provides protection against subsequent rotavirus infection and diarrhea. This research presents a new vaccine designed based on computational models. In this study, three types of epitopes are consideredlinear, conformational, and combinationalin a proposed model protein. Several studies on rotavirus vaccines have shown that VP6 and VP4 proteins are good candidates for vaccine production. In the present study, a fusion protein was designed as a new generation of rotavirus vaccines by bioinformatics analyses. This model-based study using ABCpred, BCPREDS, Bcepred, and Ellipro web servers showed that the peptide presented in this article has the necessary properties to act as a vaccine. Prediction of linear B-cell epitopes of peptides is helpful to investigate whether these peptides are able to activate humoral immunity.
机译:轮状病毒是严重腹泻病的主要病因。自然感染可防止随后的轮状病毒感染和腹泻。这项研究提出了一种基于计算模型设计的新型疫苗。在这项研究中,三种类型的表位在拟议的模型蛋白中被认为是线性的,构象的和组合的。轮状病毒疫苗的多项研究表明,VP6和VP4蛋白是疫苗生产的良好候选者。在本研究中,通过生物信息学分析将融合蛋白设计为新一代轮状病毒疫苗。这项使用ABCpred,BCPREDS,Bcepred和Ellipro Web服务器进行的基于模型的研究表明,本文介绍的肽具有用作疫苗的必要特性。肽的线性B细胞表位的预测有助于研究这些肽是否能够激活体液免疫。

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