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Novel Immunoinformatics Approaches to Design Multi-epitope Subunit Vaccine for Malaria by Investigating Anopheles Salivary Protein

机译:通过研究按蚊唾液蛋白设计用于疟疾的多表位亚单位疫苗的新型免疫信息学方法。

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摘要

Malaria fever has been pervasive for quite a while in tropical developing regions causing high morbidity and mortality. The causal organism is a protozoan parasite of genus Plasmodium which spreads to the human host by the bite of hitherto infected female Anopheles mosquito. In the course of biting, a salivary protein of Anopheles helps in blood feeding behavior and having the ability to elicit the host immune response. This study represents a series of immunoinformatics approaches to design multi-epitope subunit vaccine using Anopheles mosquito salivary proteins. Designed subunit vaccine was evaluated for its immunogenicity, allergenicity and physiochemical parameters. To enhance the stability of vaccine protein, disulfide engineering was performed in a region of high mobility. Codon adaptation and in silico cloning was also performed to ensure the higher expression of designed subunit vaccine in E. coli K12 expression system. Finally, molecular docking and simulation study was performed for the vaccine protein and TLR-4 receptor, to determine the binding free energy and complex stability. Moreover, the designed subunit vaccine was found to induce anti-salivary immunity which may have the ability to prevent the entry of Plasmodium sporozoites into the human host.
机译:在热带发展中地区,疟疾热已经普及了很长一段时间,导致高发病率和高死亡率。致病生物是疟原虫属的原生动物寄生虫,它通过迄今为止被感染的雌性按蚊的叮咬传播到人的宿主。在咬人的过程中,按蚊的唾液蛋白有助于血液供应行为,并具有引起宿主免疫反应的能力。这项研究代表了一系列免疫信息学方法,旨在使用按蚊蚊唾液蛋白设计多表位亚单位疫苗。对设计的亚单位疫苗的免疫原性,致敏性和理化参数进行了评估。为了增强疫苗蛋白的稳定性,在高迁移率区域进行了二硫键工程。还进行了密码子适应和计算机克隆,以确保设计的亚单位疫苗在大肠杆菌K12表达系统中更高的表达。最后,对疫苗蛋白和TLR-4受体进行了分子对接和模拟研究,以确定结合自由能和复合物的稳定性。而且,发现设计的亚单位疫苗诱导抗唾液免疫,其可能具有防止疟原虫子孢子进入人宿主的能力。

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