Cryo-EM structures of two bovine adenovirus type 3 intermediates

被引:30
作者
Cheng, Lingpeng [1 ]
Huang, Xiaoxing [1 ]
Li, Xiaomin [1 ]
Xiong, Wei [2 ]
Sun, Wei [1 ]
Yang, Chongwen [1 ]
Zhang, Kai [1 ]
Wang, Ying [1 ]
Liu, Hongrong [3 ]
Huang, Xiaojun [1 ]
Ji, Gang [1 ]
Sun, Fei [1 ]
Zheng, Congyi [2 ]
Zhu, Ping [1 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Natl Lab Biomacromol, Beijing 100101, Peoples R China
[2] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan 430072, Hubei, Peoples R China
[3] Hunan Normal Univ, Coll Phys & Informat Sci, Changsha 410081, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Bovine adenovirus; Adenovirus assembly; Subviral particles; Polypeptide VI; RESOLUTION CRYOELECTRON MICROSCOPY; SINGLE-PARTICLE RECONSTRUCTIONS; VIRAL-DNA; 3D RECONSTRUCTION; VACCINE VECTORS; COILED COILS; PENTON BASE; PROTEIN; SEROTYPE; REVEALS;
D O I
10.1016/j.virol.2013.12.012
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Adenoviruses (Ads) infect hosts from all vertebrate species and have been investigated as vaccine vectors. We report here near-atomic structures of two bovine Ad type 3 (BAd3) intermediates obtained by cryo-electron microscopy. A comparison between the two intermediate structures reveals that the differences are localized in the fivefold vertex region, while their facet structures are identical. The overall facet structure of BAd3 exhibits a similar structure to human Ads; however, BAd3 protein IX has a unique conformation. Mass spectrometry and cryo-electron tomography analyses indicate that one intermediate structure represents the stage during DNA encapsidation, whilst the other intermediate structure represents a later stage. These results also suggest that cleavage of precursor protein VI occurs during, rather than after, the DNA encapsidation process. Overall, our results provide insights into the mechanism of Ad assembly, and allow the first structural comparison between human and nonhuman Ads at backbone level. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:174 / 181
页数:8
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