Atomic cryo-EM structures of viruses

被引:52
作者
Jiang, Wen [1 ,2 ,3 ,4 ]
Tang, Liang [5 ]
机构
[1] Purdue Univ, Dept Biol Sci Immunol & Infect Dis, 240 S Martin Jischke Dr, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Chem Immunol & Infect Dis, 240 S Martin Jischke Dr, W Lafayette, IN 47907 USA
[3] Purdue Univ, Markey Ctr Struct Biol Immunol & Infect Dis, 240 S Martin Jischke Dr, W Lafayette, IN 47907 USA
[4] Purdue Univ, Purdue Inst Inflammat Immunol & Infect Dis, 240 S Martin Jischke Dr, W Lafayette, IN 47907 USA
[5] Univ Kansas, Dept Mol Biosci, 1200 Sunnyside Ave, Lawrence, KS 66045 USA
基金
美国国家卫生研究院;
关键词
ANISOTROPIC MAGNIFICATION DISTORTION; PARTICLE ELECTRON-MICROSCOPY; 2.9 ANGSTROM RESOLUTION; BEAM-INDUCED MOTION; IN-SITU STRUCTURES; CRYOELECTRON MICROSCOPY; 3-DIMENSIONAL STRUCTURE; CAPSID MATURATION; BACTERIOPHAGE T7; HUMAN ADENOVIRUS;
D O I
10.1016/j.sbi.2017.07.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
During the development of single particle cryo-EM in past five decades, icosahedral viruses have led the resolution progress owing to their large mass and high symmetry. Many technical advances in cryo-EM were first established with viruses. Since reaching 4 A resolution in 2008, it has become a relatively routine task to solve the atomic structure of isolated viruses. The future of structural virology will be increasingly focused on remaining challenges including solving structures of jumbo viruses, intermediate functional states during assembly, maturation, and infection, and in situ structures. Recent demonstrations of near-atomic resolution structure with electron tomography and sub-tomogram averaging opens a new direction for high resolution studies of pleomorphic viruses and the pleomorphic states of icosahedral viruses that have defied past efforts using the single particle cryo-EM approach.
引用
收藏
页码:122 / 129
页数:8
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