表位:鉴定病原体和已知免疫表位之间的分子相似性

Christian A Balbin , Janelle Nunez-Castilla , Vitalii Stebliankin , Prabin Baral , Masrur Sobhan , Trevor Cickovski , Ananda Mohan Mondal , Giri Narasimhan , Prem Chapagain , Kalai Mathee , Jessica Siltberg-Liberles
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引用次数: 0

摘要

感染后,外来抗原蛋白刺激宿主免疫系统产生针对病原体的抗体。这些抗体结合到抗原上被称为表位的区域。感染病原体与宿主蛋白或宿主先前遇到的其他致病性蛋白之间的表位结构相似性(分子模仿)可以影响宿主对病原体的免疫反应,并可能导致交叉反应性抗体。识别病原体中潜在的分子模仿区域的能力可以阐明对病原体治疗和疫苗设计特别重要的免疫效应。在这里,我们介绍了Epitopedia,这是一个软件管道,有助于识别抗原病原体蛋白和免疫表位数据库(IEDB)编目的已知免疫表位之间可能表现出潜在的三维分子模仿的区域。Epitopedia是MIT许可下发布的开源软件,在GitHub上免费提供,包括一个预先安装了所有其他软件依赖的Docker容器。我们分析了不同的二级结构状态、五肽对之间的同一性以及五肽对亲本序列之间的同一性对RMSD的影响。我们发现,螺旋构象中的五肽对的RMSD值明显低于延伸构象或螺旋构象中的RMSD值。我们还发现,当五肽对来自非同源序列时,RMSD显著增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Epitopedia: identifying molecular mimicry between pathogens and known immune epitopes

Epitopedia: identifying molecular mimicry between pathogens and known immune epitopes

Upon infection, foreign antigenic proteins stimulate the host's immune system to produce antibodies targeting the pathogen. These antibodies bind to regions on the antigen called epitopes. Structural similarity (molecular mimicry) of epitopes between an infecting pathogen and host proteins or other pathogenic proteins the host has previously encountered can impact the host immune response to the pathogen and may lead to cross-reactive antibodies. The ability to identify potential regions of molecular mimicry in a pathogen can illuminate immune effects which are especially important to pathogen treatment and vaccine design. Here we present Epitopedia, a software pipeline that facilitates the identification of regions that may exhibit potential three-dimensional molecular mimicry between an antigenic pathogen protein and known immune epitopes as catalogued by the Immune Epitope Database (IEDB). Epitopedia is open-source software released under the MIT license and is freely available on GitHub, including a Docker container with all other software dependencies preinstalled. We performed an analysis describing how various secondary structure states, identity between pentapeptide pairs, and identity between the parent sequences of pentapeptide pairs affects RMSD. We found that pentapeptides pairs in a helical conformation had considerably lower RMSD values than those in extended or coil conformations. We also found that RMSD is significantly increased when pentapeptide pairs are from non-homologous sequences.

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来源期刊
Immunoinformatics (Amsterdam, Netherlands)
Immunoinformatics (Amsterdam, Netherlands) Immunology, Computer Science Applications
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