Laboratory of Protein Engineering and Vaccines, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China.
CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Cell Rep. 2019 Jan 8;26(2):438-446.e5. doi: 10.1016/j.celrep.2018.12.065.
Yellow fever virus (YFV), a deadly human pathogen, is the prototype of the genus Flavivirus. Recently, YFV re-emerged in Africa and Brazil, leading to hundreds of deaths, with some cases imported to China. Prophylactic or therapeutic countermeasures are urgently needed. Previously, several human monoclonal antibodies against YFV were screened out by phage display. Here, we find that one of them, 5A, exhibits high neutralizing potency and good protection. Crystallographic analysis of the YFV envelope (E) protein in its pre- and post-fusion states shows conformations similar to those observed in other E proteins of flaviviruses. Furthermore, the structures of 5A in complex with the E protein in both states are resolved, revealing an invariant recognition site. Structural analysis and functional data suggest that 5A has high neutralization potency because it interferes with virus entry by preventing both virus attachment and fusion. These findings will be instrumental for immunogen or inhibitor design.
黄热病毒(YFV)是一种致命的人类病原体,是黄病毒属的原型。最近,YFV 在非洲和巴西再次出现,导致数百人死亡,并有一些病例输入中国。因此,迫切需要预防或治疗对策。以前,已经通过噬菌体展示筛选出几种针对 YFV 的人源单克隆抗体。在这里,我们发现其中一种 5A 具有很高的中和效力和良好的保护作用。YFV 包膜(E)蛋白在其融合前和融合后的晶体结构分析表明,其构象与其他黄病毒的 E 蛋白观察到的构象相似。此外,还解析了 5A 与两种状态下 E 蛋白的复合物结构,揭示了一个不变的识别位点。结构分析和功能数据表明,5A 具有很高的中和效力,因为它通过阻止病毒附着和融合来干扰病毒进入。这些发现将有助于免疫原或抑制剂的设计。