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使用EPIBOT预测巴西利什曼原虫蛋白质中的CD8 +表位:计算机模拟搜索和体内验证

Prediction of CD8+ Epitopes in Leishmania braziliensis Proteins Using EPIBOT: In Silico Search and In Vivo Validation.

作者信息

Duarte Angelo, Queiroz Artur T L, Tosta Rafael, Carvalho Augusto M, Barbosa Carlos Henrique, Bellio Maria, de Oliveira Camila I, Barral-Netto Manoel

机构信息

Departmento de Tecnologia, Universidade Estadual de Feira de Santana, Av. Transnordestina, s/n, DTEC-Módulo 3, 44036-900, Feira de Santana, BA, Brazil.

CPqGM-FIOCRUZ, R. Waldemar Falcão, 121, 40296-710, Salvador, BA, Brazil.

出版信息

PLoS One. 2015 Apr 23;10(4):e0124786. doi: 10.1371/journal.pone.0124786. eCollection 2015.

Abstract

BACKGROUND

Leishmaniasis is caused by intracellular Leishmania parasites that induce a T-cell mediated response associated with recognition of CD4+ and CD8+ T cell Line 1Lineepitopes. Identification of CD8+ antigenic determinants is crucial for vaccine and therapy development. Herein, we developed an open-source software dedicated to search and compile data obtained from currently available on line prediction algorithms.

METHODOLOGY/PRINCIPAL FINDINGS: We developed a two-phase algorithm and implemented in an open source software called EPIBOT, that consolidates the results obtained with single prediction algorithms, generating a final output in which epitopes are ranked. EPIBOT was initially trained using a set of 831 known epitopes from 397 proteins from IEDB. We then screened 63 Leishmania braziliensis vaccine candidates with the EPIBOT trained tool to search for CD8+ T cell epitopes. A proof-of-concept experiment was conducted with the top eight CD8+ epitopes, elected by EPIBOT. To do this, the elected peptides were synthesized and validated for their in vivo cytotoxicity. Among the tested epitopes, three were able to induce lysis of pulsed-target cells.

CONCLUSION

Our results show that EPIBOT can successfully search across existing prediction tools, generating a compiled list of candidate CD8+ epitopes. This software is fast and a simple search engine that can be customized to search over different MHC alleles or HLA haplotypes.

摘要

背景

利什曼病由细胞内利什曼原虫寄生虫引起,这些寄生虫会引发与识别CD4+和CD8+ T细胞表位相关的T细胞介导反应。鉴定CD8+抗原决定簇对于疫苗和治疗方法的开发至关重要。在此,我们开发了一款开源软件,专门用于搜索和汇编从当前可用的在线预测算法中获得的数据。

方法/主要发现:我们开发了一种两阶段算法,并在一款名为EPIBOT的开源软件中实现,该软件整合了使用单一预测算法获得的结果,生成一个最终输出,其中表位会被排序。EPIBOT最初使用来自免疫表位数据库(IEDB)中397种蛋白质的831个已知表位进行训练。然后,我们使用经过EPIBOT训练的工具筛选了63种巴西利什曼原虫疫苗候选物,以寻找CD8+ T细胞表位。对由EPIBOT选出的前八个CD8+表位进行了概念验证实验。为此,合成了所选肽段,并对其体内细胞毒性进行了验证。在测试的表位中,有三个能够诱导脉冲靶细胞的裂解。

结论

我们的结果表明,EPIBOT可以成功地在现有的预测工具中进行搜索,生成候选CD8+表位的汇编列表。该软件是一个快速且简单的搜索引擎,可以进行定制,以搜索不同的MHC等位基因或HLA单倍型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1250/4407964/77111eaa6b19/pone.0124786.g001.jpg

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