Program in Emerging Infectious Diseases, Duke-NUS Medical School, KTP Building, 8 College Road, Singapore, 169857, Singapore.
Centre for BioImaging Sciences, National University of Singapore, Singapore, 117557, Singapore.
Nat Commun. 2020 Jun 19;11(1):3112. doi: 10.1038/s41467-020-16925-y.
Previous flavivirus (dengue and Zika viruses) studies showed largely spherical particles either with smooth or bumpy surfaces. Here, we demonstrate flavivirus particles have high structural plasticity by the induction of a non-spherical morphology at elevated temperatures: the club-shaped particle (clubSP), which contains a cylindrical tail and a disc-like head. Complex formation of DENV and ZIKV with Fab C10 stabilize the viruses allowing cryoEM structural determination to ~10 Å resolution. The caterpillar-shaped (catSP) Fab C10:ZIKV complex shows Fabs locking the E protein raft structure containing three E dimers. However, compared to the original spherical structure, the rafts have rotated relative to each other. The helical tail structure of Fab C10:DENV3 clubSP showed although the Fab locked an E protein dimer, the dimers have shifted laterally. Morphological diversity, including clubSP and the previously identified bumpy and smooth-surfaced spherical particles, may help flavivirus survival and immune evasion.
先前的黄病毒(登革热和寨卡病毒)研究表明,大多数球形颗粒的表面要么光滑,要么粗糙。在这里,我们证明了黄病毒颗粒具有很高的结构可塑性,能够在高温下诱导形成非球形形态:棒状颗粒(clubSP),其包含一个圆柱形尾部和一个盘状头部。用 Fab C10 对 DENV 和 ZIKV 的复杂形成进行稳定化处理,使病毒能够进行 cryoEM 结构测定,分辨率达到约 10 Å。毛毛虫状(catSP)Fab C10:ZIKV 复合物显示 Fab 锁定含有三个 E 二聚体的 E 蛋白筏结构。然而,与原始的球形结构相比,筏已相对彼此旋转。Fab C10:DENV3 clubSP 的螺旋状尾部结构表明,尽管 Fab 锁定了一个 E 蛋白二聚体,但二聚体已横向移位。形态多样性,包括 clubSP 和之前鉴定的粗糙和光滑表面的球形颗粒,可能有助于黄病毒的存活和免疫逃逸。