免疫信息学驱动的多表位疫苗设计有效保护马丘波病毒。

IF 3.8 2区 化学 Q2 CHEMISTRY, APPLIED
Abdulaziz Alamri, Saeedah Almutairi, Salman Al Rokayan, Mohamed Y Zaky, Mostafa A Abdel-Maksoud, Israr Fatima
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引用次数: 0

摘要

沙病毒科病毒包括马丘波病毒(MACV),它与可能致命的玻利维亚出血热有关,这种疾病的死亡率为15%-30%,具体取决于诊断速度和卫生设施的可用性。迄今为止,还没有获得许可的MACV疫苗,这突出了采取预防措施的必要性。在这项工作中,我们使用免疫信息学方法创建基于最显性MACV蛋白的多表位疫苗。对于构建性表位,我们选择了糖蛋白前体(GP)、核蛋白(NP)、RNA依赖RNA聚合酶(L)和锌结合环指蛋白(Z),以获取复制和入侵宿主细胞所必需的蛋白质。使用计算机预测方法,共有13个t细胞表位(7个MHC I类和6个MHC II类结合物)和8个b细胞表位被鉴定为具有最大潜力引发强而广谱的免疫反应。这些选择的表位经过计算机验证,以确保最高程度的免疫原性和无过敏性或毒性作用。为了增加疫苗引发免疫反应的可能性,将50S核糖体蛋白L7/L12作为佐剂添加。人群覆盖率分析表明,该抗原表位可为世界近98.04%的人口提供免疫保护。理论疫苗设计包括三维建模和模拟与toll样受体4 (TLR4)和MHC分子等免疫受体的对接,证实了它们稳定且高亲和力的结合相互作用。免疫反应的计算机模拟结果也显示了大量抗体的产生和各种t细胞亚群的强烈参与。总之,本研究提出了一种多表位马丘波病毒候选疫苗,可以在实验室进行测试,以评估其作为玻利维亚出血热预防措施的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunoinformatics-driven design of a multi-epitope vaccine for effective protection against Machupo virus.

The Arenaviridae family of viruses includes the Machupo virus (MACV), which is associated with the potentially fatal Bolivian hemorrhagic fever, a disease with a mortality rate of 15%-30% depending on the speed of diagnosis and the availability of health facilities. To date, there is no licensed vaccine available for MACV, highlighting the need for a preventive measure. In this work, we use immunoinformatics approaches to create a multi-epitope vaccine based on the most dominant MACV proteins. For constructational epitopes, we selected glycoprotein precurssor (GP), nucleoprotein (NP), RNA-dependant RNA polymerase (L), and Zinc-binding RING finger protein (Z) from garner the proteins essential for replicating and invading a host cell. Using in silico prediction methods, a total of thirteen T-cell epitopes (seven MHC class I and six MHC class II binders) and eight B-cell epitopes were identified as having the greatest potential to elicit strong and broad-spectrum immune responses. These selected epitopes were validated in silico to ensure the highest degree of immunogenicity and no allergenic or toxic effects. To increase the potential of the vaccine to elicit an immune response, the 50S ribosomal protein L7/L12 was added as an adjuvant. The analysis of population coverage indicated that the epitopes could provide immunological protection to nearly 98.04% of the world population. The theoretical vaccine design included 3D modeling and simulation of docking to immunoreceptors like Toll-like receptor 4 (TLR4) and MHC molecules, which confirmed their stable and high-affinity binding interactions. The results from in silico simulations of the immune response also showed abundant production of antibodies and strong engagement of various T-cell subsets. In summary, this study proposes a multi-epitope Machupo virus vaccine candidate that can be tested in the lab to evaluate its effectiveness as a preventative measure for Bolivian hemorrhagic fever.

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来源期刊
Molecular Diversity
Molecular Diversity 化学-化学综合
CiteScore
7.30
自引率
7.90%
发文量
219
审稿时长
2.7 months
期刊介绍: Molecular Diversity is a new publication forum for the rapid publication of refereed papers dedicated to describing the development, application and theory of molecular diversity and combinatorial chemistry in basic and applied research and drug discovery. The journal publishes both short and full papers, perspectives, news and reviews dealing with all aspects of the generation of molecular diversity, application of diversity for screening against alternative targets of all types (biological, biophysical, technological), analysis of results obtained and their application in various scientific disciplines/approaches including: combinatorial chemistry and parallel synthesis; small molecule libraries; microwave synthesis; flow synthesis; fluorous synthesis; diversity oriented synthesis (DOS); nanoreactors; click chemistry; multiplex technologies; fragment- and ligand-based design; structure/function/SAR; computational chemistry and molecular design; chemoinformatics; screening techniques and screening interfaces; analytical and purification methods; robotics, automation and miniaturization; targeted libraries; display libraries; peptides and peptoids; proteins; oligonucleotides; carbohydrates; natural diversity; new methods of library formulation and deconvolution; directed evolution, origin of life and recombination; search techniques, landscapes, random chemistry and more;
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