Prediction of Multiple Peptide Based Vaccine from E1, E2 and Capsid Proteins of Rubella Virus: An In-Silico Approach

Shaima N. Elgenaid, Ebrahim Mohammed Al-Hajj, A. Ibrahim, M. Essa, Ahmed Hamdi Abu-haraz, K. A. Abd-elrahman, Mohamed A. Hassan
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引用次数: 6

Abstract

Rubella is a single strand RNA virus in structure that belongs to Togaviridae family. It causes rubella by respiratory droplet transmission and congenital rubella syndrome if infection to the mother occurs during pregnancy. The current life attenuated vaccine is given as part of MMR vaccine. It has many side effects and contraindicated in pregnancy and immunosuppressed persons. The aim of this study is to determine antigenic peptides from E1, E2, and Capsid proteins that can be used for multiple peptide vaccine design using In-Silico study. A total of 189 sequences of three proteins were obtained from NCBI and subjected to multiple sequence alignments using CLUSTALW tool to determine conserved regions. Immune Epitope Data Base tools were used to determine B cell epitopes, these tools are Bepipred Linear B cell epitopes prediction, surface accessibility and antigenicity prediction. Epitope binding to MHC class I and class II and their population coverage were also determined using IEDB software. The analysis results are as follow, for B cell binding from E1 were (PVCQRHSP, QYHPTAC, and QVPPD), from E2 (AQYPP, PAHP and TTAANSTTAATPATA), and (PPPP, PPQQPQPP and PPHT) from capsid protein. All these peptides have high score in Linear B cell epitopes prediction, surface accessibility and antigenicity prediction. On another hand peptides that reacted to MHC class I were (YFNPGGSYY, FVLLVPWVL and FTNLGTPPL) form E1, E2 and capsid protein respectively. It worth noting that the peptide FVLLVPWVL from E2 protein is also binds to MHC class II with high affinity. All T cell peptides had highest population coverage, and the combined coverage for all peptides in this study was found to be 100%. Using In-Silico studies will ensure less risk of virulence and side effects. Evaluation of antibodies response in animal models is needed to confirm efficacy of these epitopes in inducing protective immune response.
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基于风疹病毒E1、E2和衣壳蛋白的多肽疫苗的预测:一种计算机方法
风疹是一种单链RNA病毒,在结构上属于风疹病毒科。它通过呼吸道飞沫传播引起风疹,如果母亲在怀孕期间感染,则会引起先天性风疹综合征。目前的生命减毒疫苗是作为MMR疫苗的一部分给予的。有许多副作用,孕妇及免疫抑制者禁用。本研究的目的是通过in - silicon研究从E1、E2和衣壳蛋白中确定可用于多肽疫苗设计的抗原肽。从NCBI中获得3种蛋白共189个序列,使用CLUSTALW工具进行多次序列比对,确定保守区。免疫表位数据库工具用于B细胞表位的测定,这些工具包括Bepipred线性B细胞表位预测、表面可及性和抗原性预测。用IEDB软件测定MHC I类和II类表位结合及其种群覆盖率。分析结果如下:B细胞结合E1为(PVCQRHSP、QYHPTAC、QVPPD),结合E2为(AQYPP、PAHP、TTAANSTTAATPATA),结合衣壳蛋白PPPP、PPQQPQPP、PPHT。这些肽在线性B细胞表位预测、表面可及性和抗原性预测方面均有较高的评分。另一方面,与MHC I类反应的肽分别形成E1、E2和衣壳蛋白(YFNPGGSYY、FVLLVPWVL和FTNLGTPPL)。值得注意的是,E2蛋白中的肽FVLLVPWVL也以高亲和力与MHC II类结合。所有的T细胞肽具有最高的群体覆盖率,并且本研究中所有肽的综合覆盖率为100%。使用芯片研究将确保降低毒性和副作用的风险。需要在动物模型中对抗体反应进行评估,以确认这些表位在诱导保护性免疫反应方面的功效。
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