表位
脚手架
马蹄蟹
病毒学
计算生物学
生物
免疫学
医学
抗原
生物医学工程
生态学
作者
Fangxin Zhao,Yue Zhang,Zhiling Zhang,Zhengshan Chen,Xiaolin Wang,Shaoyan Wang,Ruihua Li,Yaohui Li,Zhang Zhang,Wanru Zheng,Yudong Wang,Qishan Wang,Shipo Wu,Yilong Yang,Jing Zhang,Xiaodong Zai,Junjie Xu,Wei Chen
标识
DOI:10.1186/s12951-025-03200-9
摘要
The continuous emergence of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variants highlights the need to update coronavirus 2019 disease (COVID-19) vaccine components. Epitope-based vaccine designs targeting conserved and immunorecessive regions of SARS-CoV-2 are critically needed. Here, we report an engineered epitope-focused immunogen design based on a novel horseshoe-shaped natural protein scaffold, named ribonuclease inhibitor 1 (RNH1), that can multiply display of conserved neutralizing epitopes from SARS-CoV-2 S2 stem helix. The designed immunogen RNH1-S1139 demonstrates high binding affinity to S2-specific neutralizing antibodies and elicits robust epitope-targeted antibody responses either through homologous or heterologous vaccination regimens. RNH1-S1139 immune serum has been proven to have similar binding ability against SARS-CoV, SARS-CoV-2 and its variants, providing broad-spectrum protection as a membrane fusion inhibitor. Further studies showed that RNH1 has the potential to serve as a versatile scaffold that displays other helical epitopes from various antigens, including respiratory syncytial virus (RSV) F glycoprotein. Our proposed immunogen engineering strategy via tailored horseshoe-shape nano-scaffold supports the continued development of epitope-focused vaccines as part of a next-generation vaccine design.
科研通智能强力驱动
Strongly Powered by AbleSci AI