一种构建嵌合蛋白的计算机方法,靶向志贺菌的毒力因子。

Q4 Pharmacology, Toxicology and Pharmaceutics International Journal of Computational Biology and Drug Design Pub Date : 2018-11-14 DOI:10.1504/IJCBDD.2018.10017410
Emad Kordbacheh, S. Nazarian, Amin Farhang
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引用次数: 0

摘要

志贺菌病是一种高负担的胃肠道疾病,抗生素耐药性增加。III型分泌器(T3SA)在不同种类的志贺菌中是保守的;IpaD、IpaB和IcsA蛋白参与其功能。研究表明志贺毒素作为一种毒力因子在出血性结肠炎中具有重要作用。为此目的招募了生物信息学工具。在核小体水平、序列选择和优化以及转录组阶段,一些与mRNA形式相关的预测,也在蛋白质组、物理化学参数、最佳稳定性、第一到第三结构和模型验证的步骤中,是在计算机服务器的帮助下进行的一些预测。此外,通过生物信息学软件估计抗原和致敏倾向、亚细胞定位和蛋白质功能。最后,这些结果将有益于开发针对志贺菌属的普遍候选免疫原的动物模型。
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An in silico approach for construction of a chimeric protein, targeting virulence factors of Shigella spp.
Shigellosis is a high burden gastrointestinal disease with an increased frequency of antibiotic resistance. Type III secretion apparatus (T3SA) are conserved among different species of Shigella; and IpaD, IpaB, and IcsA proteins participate in its function. Studies indicate shiga toxin as a virulence factor has a fundamental role in hemorrhagic colitis. Bioinformatics tools were recruited for aiding this purpose. In the level of the nucleosome, sequences choosing and optimising and in the phase of the transcriptome, some prediction in associate with mRNA form, also in step of the proteome, physicochemical parameter, best stability, first to third structures and model validation were some prediction performed in assistance with in silico servers. Moreover, estimating antigenic and allergenic propensity, subcellular localisation and protein function were accomplished by bioinformatics software. Finally, these results would be beneficial in an animal model purpose for development of a pervasive candidate immunogen against Shigella spp.
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来源期刊
International Journal of Computational Biology and Drug Design
International Journal of Computational Biology and Drug Design Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.00
自引率
0.00%
发文量
8
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