Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.
Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX 78712, USA.
Curr Opin Immunol. 2022 Aug;77:102209. doi: 10.1016/j.coi.2022.102209. Epub 2022 May 19.
Viral proteins fold into a variety of structures as they perform their functions. Structure-based vaccine design aims to exploit knowledge of an antigen's architecture to stabilize it in a vulnerable conformation. We summarize the general principles of structure-based vaccine design, with a focus on the major types of sequence modifications: proline, disulfide, cavity-filling, electrostatic and hydrogen-bond substitution, as well as domain deletion. We then review recent applications of these principles to vaccine-design efforts across five viral families: Coronaviridae, Orthomyxoviridae, Paramyxoviridae, Pneumoviridae, and Filoviridae. Outstanding challenges include continued application of proven design principles to pathogens of interest, as well as development of new strategies for those pathogens that resist traditional techniques.
病毒蛋白在执行其功能时会折叠成多种结构。基于结构的疫苗设计旨在利用抗原结构的知识来稳定其脆弱构象。我们总结了基于结构的疫苗设计的一般原则,重点介绍了主要类型的序列修饰:脯氨酸、二硫键、腔填充、静电和氢键取代以及结构域缺失。然后,我们回顾了这些原则在五个病毒科的疫苗设计工作中的最新应用:冠状病毒科、正粘病毒科、副粘病毒科、肺病毒科和丝状病毒科。突出的挑战包括将经过验证的设计原则持续应用于相关病原体,以及为那些抵制传统技术的病原体开发新策略。