通过电子冷冻显微镜揭示的传染性ε15病毒衣壳的骨干结构。

Backbone structure of the infectious epsilon15 virus capsid revealed by electron cryomicroscopy.

作者信息

Jiang Wen, Baker Matthew L, Jakana Joanita, Weigele Peter R, King Jonathan, Chiu Wah

机构信息

Markey Center for Structural Biology, Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

Nature. 2008 Feb 28;451(7182):1130-4. doi: 10.1038/nature06665.

Abstract

A half-century after the determination of the first three-dimensional crystal structure of a protein, more than 40,000 structures ranging from single polypeptides to large assemblies have been reported. The challenge for crystallographers, however, remains the growing of a diffracting crystal. Here we report the 4.5-A resolution structure of a 22-MDa macromolecular assembly, the capsid of the infectious epsilon15 (epsilon15) particle, by single-particle electron cryomicroscopy. From this density map we constructed a complete backbone trace of its major capsid protein, gene product 7 (gp7). The structure reveals a similar protein architecture to that of other tailed double-stranded DNA viruses, even in the absence of detectable sequence similarity. However, the connectivity of the secondary structure elements (topology) in gp7 is unique. Protruding densities are observed around the two-fold axes that cannot be accounted for by gp7. A subsequent proteomic analysis of the whole virus identifies these densities as gp10, a 12-kDa protein. Its structure, location and high binding affinity to the capsid indicate that the gp10 dimer functions as a molecular staple between neighbouring capsomeres to ensure the particle's stability. Beyond epsilon15, this method potentially offers a new approach for modelling the backbone conformations of the protein subunits in other macromolecular assemblies at near-native solution states.

摘要

在确定了蛋白质的首个三维晶体结构半个世纪后,已报道了4万多种结构,范围从单条多肽链到大型组装体。然而,晶体学家面临的挑战仍然是生长出能产生衍射的晶体。在此,我们通过单颗粒冷冻电子显微镜技术报道了一种22兆道尔顿大分子组装体——感染性ε15(ε15)病毒颗粒的衣壳——的4.5埃分辨率结构。根据这个密度图,我们构建了其主要衣壳蛋白基因产物7(gp7)的完整主链轨迹。该结构揭示出与其他有尾双链DNA病毒相似的蛋白质结构,即便不存在可检测到的序列相似性。然而,gp7中二级结构元件的连接性(拓扑结构)是独特的。在二重对称轴周围观察到了无法用gp7解释的突出密度。随后对整个病毒进行的蛋白质组学分析将这些密度鉴定为gp10,一种12千道尔顿的蛋白质。其结构、位置以及与衣壳的高结合亲和力表明,gp10二聚体作为相邻衣壳粒之间的分子订书钉发挥作用,以确保病毒颗粒的稳定性。除了ε15病毒,这种方法有可能为在接近天然溶液状态下模拟其他大分子组装体中蛋白质亚基的主链构象提供一种新方法。

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