Principles and practical applications of structure-based vaccine design

被引:24
|
作者
Byrne, Patrick O. [1 ]
McLellan, Jason S. [1 ]
机构
[1] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
关键词
INTERMOLECULAR DISULFIDE BOND; TYPE-1 ENVELOPE GLYCOPROTEIN; COILED COILS; AMINO-ACIDS; PROTEIN; SPIKE; GP120; MUTATIONS; STABILITY; RESPONSES;
D O I
10.1016/j.coi.2022.102209
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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, cavityfilling, 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: 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.
引用
收藏
页数:9
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