Pantelic Radosav S, Lockett Linda J, Rothnagel Rosalba, Hankamer Ben, Both Gerald W
Institute for Molecular Bioscience, University of Queensland, Brisbane, Queensland 4072, Australia.
J Virol. 2008 Aug;82(15):7346-56. doi: 10.1128/JVI.00764-08. Epub 2008 May 28.
A three-dimensional (3D) cryoelectron microscopy reconstruction of the prototype Atadenovirus (OAdV [an ovine adenovirus isolate]) showing information at a 10.6-A resolution (0.5 Fourier shell correlation) was derived by single-particle analysis. This is the first 3D structure solved for any adenovirus that is not a Mastadenovirus, allowing cross-genus comparisons between structures and the assignment of genus-specific capsid proteins. Viable OAdV mutants that lacked the genus-specific LH3 and p32k proteins in purified virions were also generated. Negatively stained 3D reconstructions of these mutants were used to identify the location of protein LH3 and infer that of p32k within the capsid. The key finding was that LH3 is a critical protein that holds the outer capsid of the virus together. In its absence, the outer viral capsid is unstable. LH3 is located in the same position among the hexon subunits as its protein IX equivalent from mastadenoviruses but sits on top of the hexon trimers, forming prominent "knobs" on the virion surface that visually distinguish OAdV from other known AdVs. Electron density was also assigned to hexon and penton subunits and to proteins IIIa and VIII. There was good correspondence between OAdV density and human AdV hexon structures, which also validated the significant differences that were observed between the penton base protein structures.
通过单颗粒分析,获得了原型腺病毒(OAdV [一种绵羊腺病毒分离株])的三维(3D)冷冻电子显微镜重建结构,其分辨率为10.6埃(0.5傅里叶壳层相关系数)。这是首个解析出的非哺乳动物腺病毒的3D结构,使得不同属病毒的结构之间能够进行跨属比较,并可对属特异性衣壳蛋白进行归属。还构建了纯化病毒粒子中缺乏属特异性LH3和p32k蛋白的活OAdV突变体。对这些突变体进行负染3D重建,以确定蛋白LH3的位置,并推断p32k在衣壳中的位置。关键发现是,LH3是一种关键蛋白,它将病毒的外衣壳维系在一起。没有它,病毒的外衣壳就不稳定。LH3在六邻体亚基中的位置与其在哺乳动物腺病毒中的蛋白IX等同物相同,但位于六邻体三聚体的顶部,在病毒粒子表面形成突出的“瘤”,从视觉上使OAdV与其他已知腺病毒区分开来。电子密度还被归属到六邻体和五邻体亚基以及蛋白IIIa和VIII上。OAdV密度与人腺病毒六邻体结构之间存在良好的对应关系,这也验证了在五邻基体蛋白结构中观察到的显著差异。