Structure of Sputnik, a virophage, at 3.5-Å resolution

被引:68
作者
Zhang, Xinzheng [1 ]
Sun, Siyang [1 ]
Xiang, Ye [1 ]
Wong, Jimson [1 ]
Klose, Thomas [1 ]
Raoult, Didier [2 ]
Rossmann, Michael G. [1 ]
机构
[1] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
[2] Univ Aix Marseille 2, CNRS, Inst Rech Dev 198,Fac Med, Unite Rech Malad Infect & Trop Emergentes,UMR 623, F-13385 Marseille 5, France
基金
美国国家卫生研究院;
关键词
dsDNA egress; virus assembly; Mimivirus satellite; polypeptide tracing; cryo-electron microscopy; 3-DIMENSIONAL STRUCTURE; BACTERIOPHAGE PRD1; FUNCTIONAL IMPLICATIONS; CRYSTAL-STRUCTURE; CAPSID PROTEIN; MOSAIC-VIRUS; ADENOVIRUS; EVOLUTION; MIMIVIRUS; INTERNALIZATION;
D O I
10.1073/pnas.1211702109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
"Sputnik" is a dsDNA virus, referred to as a virophage, that is coassembled with Mimivirus in the host amoeba. We have used cryo-EM to produce an electron density map of the icosahedral Sputnik virus at 3.5-angstrom resolution, sufficient to verify the identity of most amino acids in the capsid proteins and to establish the identity of the pentameric protein forming the fivefold vertices. It was also shown that the virus lacks an internal membrane. The capsid is organized into a T = 27 lattice in which there are 260 trimeric capsomers and 12 pentameric capsomers. The trimeric capsomers consist of three double "jelly-roll" major capsid proteins creating pseudohexameric capsomer symmetry. The pentameric capsomers consist of five single jelly-roll proteins. The release of the genome by displacing one or more of the pentameric capsomers may be the result of a low-pH environment. These results suggest a mechanism of Sputnik DNA ejection that probably also occurs in other big icosahedral double jelly-roll viruses such as Adenovirus. In this study, the near-atomic resolution structure of a virus has been established where crystallization for X-ray crystallography was not feasible.
引用
收藏
页码:18431 / 18436
页数:6
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