基于硅肽的丙型肝炎病毒疫苗

V. Kaushik, Joginder Singh, Nidhi Sharma
{"title":"基于硅肽的丙型肝炎病毒疫苗","authors":"V. Kaushik, Joginder Singh, Nidhi Sharma","doi":"10.1109/BSB.2016.7552119","DOIUrl":null,"url":null,"abstract":"Hepatitis C is a severe disease caused by Hepatitis C virus which leads to human fatality and affected 180 million people across the globe. Its chronic infection leads to liver damage and malignant hepatoma. Till now there is no vaccine in the market for this virus. The objective of the study was to predict the best epitope using Bioinformatics tools for designing a vaccine against HCV. Here T-cell epitope was considered since it can recognize only antigen that processes to generate peptide by antigen presenting cell. For selecting the best T cell epitope, the binding energy with the MHC molecule must be high, must have a protease cleavage site, conserved site, motif, good binder with hydrophobic binding pocket and half-life of dissociation must be high. By considering above criteria suitable bioinformatics tools were used to predict the epitopes from NS3, NS5A and NS5B of 3a and 3b genotype. A total of 600 epitopes from different tools for each protein were predicted and from there only 11 efficient epitopes was virtually screened out using protein-protein interaction between MHC-I and MHC-II molecules and their energy. IMYAPTIWV peptide of NS5A protein was found to be the best epitope. The selected epitope for T-cell can further be used for future work in a wet laboratory for the development of vaccine against HCV.","PeriodicalId":363820,"journal":{"name":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","volume":"116 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"In silico peptide based vaccine against hepatitis C virus\",\"authors\":\"V. Kaushik, Joginder Singh, Nidhi Sharma\",\"doi\":\"10.1109/BSB.2016.7552119\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hepatitis C is a severe disease caused by Hepatitis C virus which leads to human fatality and affected 180 million people across the globe. Its chronic infection leads to liver damage and malignant hepatoma. Till now there is no vaccine in the market for this virus. The objective of the study was to predict the best epitope using Bioinformatics tools for designing a vaccine against HCV. Here T-cell epitope was considered since it can recognize only antigen that processes to generate peptide by antigen presenting cell. For selecting the best T cell epitope, the binding energy with the MHC molecule must be high, must have a protease cleavage site, conserved site, motif, good binder with hydrophobic binding pocket and half-life of dissociation must be high. By considering above criteria suitable bioinformatics tools were used to predict the epitopes from NS3, NS5A and NS5B of 3a and 3b genotype. A total of 600 epitopes from different tools for each protein were predicted and from there only 11 efficient epitopes was virtually screened out using protein-protein interaction between MHC-I and MHC-II molecules and their energy. IMYAPTIWV peptide of NS5A protein was found to be the best epitope. The selected epitope for T-cell can further be used for future work in a wet laboratory for the development of vaccine against HCV.\",\"PeriodicalId\":363820,\"journal\":{\"name\":\"2016 International Conference on Bioinformatics and Systems Biology (BSB)\",\"volume\":\"116 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-03-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2016 International Conference on Bioinformatics and Systems Biology (BSB)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/BSB.2016.7552119\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2016 International Conference on Bioinformatics and Systems Biology (BSB)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BSB.2016.7552119","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

丙型肝炎是由丙型肝炎病毒引起的一种严重疾病,可导致人类死亡,全球有1.8亿人受到影响。慢性感染可导致肝损伤和恶性肝癌。到目前为止,市场上没有针对这种病毒的疫苗。该研究的目的是利用生物信息学工具预测HCV疫苗设计的最佳表位。这里考虑t细胞表位,因为它只能识别抗原呈递细胞产生肽的抗原。为了选择最佳的T细胞表位,与MHC分子的结合能必须高,必须具有蛋白酶裂解位点、保守位点、基序、具有疏水结合袋的良好结合剂和高的解离半衰期。结合上述标准,采用合适的生物信息学工具预测3a和3b基因型的NS3、NS5A和NS5B的表位。从不同的工具中预测了每种蛋白质的总共600个表位,从中只有11个有效的表位通过MHC-I和MHC-II分子之间的蛋白质相互作用及其能量进行了虚拟筛选。发现NS5A蛋白的IMYAPTIWV肽是最佳的表位。选定的t细胞表位可进一步用于未来在湿实验室开发抗HCV疫苗的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In silico peptide based vaccine against hepatitis C virus
Hepatitis C is a severe disease caused by Hepatitis C virus which leads to human fatality and affected 180 million people across the globe. Its chronic infection leads to liver damage and malignant hepatoma. Till now there is no vaccine in the market for this virus. The objective of the study was to predict the best epitope using Bioinformatics tools for designing a vaccine against HCV. Here T-cell epitope was considered since it can recognize only antigen that processes to generate peptide by antigen presenting cell. For selecting the best T cell epitope, the binding energy with the MHC molecule must be high, must have a protease cleavage site, conserved site, motif, good binder with hydrophobic binding pocket and half-life of dissociation must be high. By considering above criteria suitable bioinformatics tools were used to predict the epitopes from NS3, NS5A and NS5B of 3a and 3b genotype. A total of 600 epitopes from different tools for each protein were predicted and from there only 11 efficient epitopes was virtually screened out using protein-protein interaction between MHC-I and MHC-II molecules and their energy. IMYAPTIWV peptide of NS5A protein was found to be the best epitope. The selected epitope for T-cell can further be used for future work in a wet laboratory for the development of vaccine against HCV.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信