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利用免疫信息学预测抗[具体对象未给出]的肽疫苗制剂的潜在表位。

Prediction of Potential Epitopes for Peptide Vaccine Formulation Against Using Immunoinformatics.

作者信息

Barman Antara, Deb Bornali, Chakraborty Supriyo

机构信息

Department of Biotechnology, Assam University, Silchar, Assam 788011 India.

出版信息

Int J Pept Res Ther. 2020;26(2):1137-1146. doi: 10.1007/s10989-019-09916-1. Epub 2019 Aug 16.

DOI:10.1007/s10989-019-09916-1
PMID:32435170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7223446/
Abstract

belongs to the family Picornaviridae and is a causal agent of the disease Teschovirus encephalomyelitis and other infections that remain asymptomatic. The present study was performed to design epitope-based peptide vaccine against by identifying the potential T cell and B-cell epitopes from capsid proteins (VP1, VP3 and VP2) of the virus using reverse vaccinology and immunoinformatics approaches. In the current study, hexapeptide T-cell and octapeptide B-cell epitopes were analyzed for immunogenicity, antigenicity and hydrophilicity scores of each epitope. Each potential epitope was further characterized using ExPASy-ProtParam and Antimicrobial Peptide Database (APD3) tools for determining various physical and chemical parameters of the epitope. One linear hexapeptide T-cell epitope, i.e., RPVNDE (epitope position 77-82) and one linear octapeptide B-cell epitope, i.e., AYSRSHPQ (236-243) were identified from the viral capsid protein as they possess the capability to raise effective immunogenic reaction in the host organism against the virus. Pharmaceutical industries could harness the results of this investigation to develop epitope-based peptide vaccines by loading the identified epitopes in combination with targeting signal peptides of T-cells and B-cells and then inserting the combination into virus like particle (vlp) or constructing subunit vaccines for further trial.

摘要

属于小核糖核酸病毒科,是猪捷申病毒脑脊髓炎及其他无症状感染的病原体。本研究旨在通过反向疫苗学和免疫信息学方法,从该病毒的衣壳蛋白(VP1、VP3和VP2)中鉴定潜在的T细胞和B细胞表位,设计针对该病毒的基于表位的肽疫苗。在本研究中,分析了六肽T细胞表位和八肽B细胞表位的免疫原性、抗原性和亲水性得分。使用ExPASy-ProtParam和抗菌肽数据库(APD3)工具进一步表征每个潜在表位,以确定表位的各种物理和化学参数。从病毒衣壳蛋白中鉴定出一个线性六肽T细胞表位,即RPVNDE(表位位置77-82)和一个线性八肽B细胞表位,即AYSRSHPQ(236-243),因为它们有能力在宿主生物体中引发针对该病毒的有效免疫反应。制药行业可以利用本研究结果,通过将鉴定出的表位与T细胞和B细胞的靶向信号肽结合,然后将该组合插入病毒样颗粒(VLP)或构建亚单位疫苗进行进一步试验,来开发基于表位的肽疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/6237ef73296f/10989_2019_9916_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/2229c551a7ab/10989_2019_9916_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/7bb328f401c5/10989_2019_9916_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/6237ef73296f/10989_2019_9916_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/2229c551a7ab/10989_2019_9916_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/7bb328f401c5/10989_2019_9916_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b42/7223446/6237ef73296f/10989_2019_9916_Fig3_HTML.jpg

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