免疫原性
抗原
病毒学
模块化设计
计算生物学
生物
抗体
穗蛋白
免疫
病毒
纳米技术
中和抗体
冠状病毒
化学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
大流行
蛋白质工程
流感疫苗
嵌合抗原受体
2019年冠状病毒病(COVID-19)
细胞生物学
融合蛋白
免疫系统
2019-20冠状病毒爆发
纳米颗粒
作者
Seojung Lee,Yejin Jang,Yujin Kim,Yumi Shin,J. W. Song,Jin Hee Ahn,Sangyong Jon
标识
DOI:10.1002/advs.202513431
摘要
The COVID-19 pandemic has underscored the urgent need for deployable vaccine platforms capable of rapidly responding to emerging and re-emerging variants of human coronaviruses. BP26, an outer membrane protein of the zoonotic bacterium Brucella, self-assembles into a highly ordered, barrel-like nanoparticle that can serve as a vaccine platform, demonstrating immunogenicity against the influenza virus and cancer when combined with specific antigens. Here, we expanded its versatility by incorporating the SpyTag/SpyCatcher pair, enabling modular and site-specific antigen conjugation via simple mixing. SpyCatcher was genetically fused to BP26, and SpyTag to the receptor binding domain (RBD) of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein, generating RBD-displaying BP26 nanoparticles (BP26-RBD). Immunization of mice with BP26-RBD elicited strong RBD-specific and neutralizing antibody responses and conferred protection against lethal SARS-CoV-2 challenge. This plug-and-play nanoparticle design supports antigen production in diverse expression systems, retains antigenic structure, and allows multivalent display, providing a cost-effective and rapidly adaptable strategy for next-generation vaccines targeting evolving viral threats.
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