Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Khartoum, Khartoum, Sudan.
Department of Biotechnology, College of Industrial and Applied Sciences, University of Bahri, Khartoum, Sudan.
Sci Rep. 2022 Sep 25;12(1):15983. doi: 10.1038/s41598-022-20397-z.
While mankind is still dealing with the COVID-19 pandemic, a case of monkeypox virus (MPXV) has been reported to the WHO on May 7, 2022. Monkeypox is a viral zoonotic disease that has been a public health threat, particularly in Africa. However, it has recently expanded to other parts of the world, so it may soon become a global issue. Thus, the current work was planned and then designed a multi-epitope vaccine against MPXV utilizing the cell surface-binding protein as a target in order to develop a novel and safe vaccine that can evoke the desirable immunological response. The proposed MHC-I, MHC-II, and B-cell epitopes were selected to design multi-epitope vaccine constructs linked with suitable linkers in combination with different adjuvants to enhance the immune responses for the vaccine constructs. The proposed vaccine was composed of 275 amino acids and was shown to be antigenic in Vaxijen server (0.5311) and non-allergenic in AllerTop server. The 3D structure of the designed vaccine was predicted, refined and validated by various in silico tools to assess the stability of the vaccine. Moreover, the solubility of the vaccine construct was found greater than the average solubility provided by protein-Sol server which indicating the solubility of the vaccine construct. Additionally, the most promising epitopes bound to MHC I and MHC II alleles were found having good binding affinities with low energies ranging between - 7.0 and - 8.6 kcal/mol. According to the immunological simulation research, the vaccine was found to elicit a particular immune reaction against the monkeypox virus. Finally, the molecular dynamic study shows that the designed vaccine is stable with minimum RMSF against MHC I allele. We conclude from our research that the cell surface-binding protein is one of the primary proteins involved in MPXV pathogenesis. As a result, our study will aid in the development of appropriate therapeutics and prompt the development of future vaccines against MPXV.
当人类仍在应对 COVID-19 大流行时,2022 年 5 月 7 日向世界卫生组织报告了一例猴痘病毒(MPXV)病例。猴痘是一种病毒性人畜共患病,一直是公共卫生威胁,特别是在非洲。然而,它最近已经扩展到世界其他地区,因此它可能很快成为一个全球性问题。因此,目前的工作是计划和设计一种针对 MPXV 的多表位疫苗,利用细胞表面结合蛋白作为靶点,以开发一种新型安全的疫苗,能够引起理想的免疫反应。选择了拟议的 MHC-I、MHC-II 和 B 细胞表位,以设计与不同佐剂结合的多表位疫苗构建体,以增强疫苗构建体的免疫反应。所提出的疫苗由 275 个氨基酸组成,在 Vaxijen 服务器(0.5311)中显示为抗原性,在 AllerTop 服务器中显示为非变应原性。设计的疫苗的 3D 结构通过各种计算机工具进行预测、精炼和验证,以评估疫苗的稳定性。此外,发现疫苗构建体的溶解度大于蛋白溶解度服务器提供的平均溶解度,这表明疫苗构建体的溶解度。此外,与 MHC I 和 MHC II 等位基因结合的最有前途的表位具有良好的结合亲和力,能量范围在-7.0 至-8.6 kcal/mol 之间。根据免疫模拟研究,发现该疫苗能针对猴痘病毒引发特定的免疫反应。最后,分子动力学研究表明,设计的疫苗对 MHC I 等位基因具有最小的 RMSF 稳定性。我们从研究中得出结论,细胞表面结合蛋白是 MPXV 发病机制中涉及的主要蛋白之一。因此,我们的研究将有助于开发适当的治疗方法,并促使开发针对 MPXV 的未来疫苗。