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Cryo-EM: beyond the microscope
被引:72
|作者:
Earl, Lesley A.
[1
]
Falconieri, Veronica
[1
]
Milne, Jacqueline L. S.
[1
]
Subramaniam, Sriram
[1
]
机构:
[1] NCI, Cell Biol Lab, Ctr Canc Res, NIH, Bldg 37, Bethesda, MD 20892 USA
基金:
美国国家卫生研究院;
关键词:
CRYOELECTRON MICROSCOPY;
ATOMIC-STRUCTURE;
STRUCTURAL BASIS;
MACROMOLECULAR COMPLEXES;
MEMBRANE-PROTEINS;
SELECTIVE CAPTURE;
CHANNEL;
ARCHITECTURE;
MECHANISM;
INSIGHTS;
D O I:
10.1016/j.sbi.2017.06.002
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:
The pace at which cryo-EM is being adopted as a mainstream tool in structural biology has continued unabated over the past year. Initial successes in obtaining near-atomic resolution structures with cryo-EM were enabled to a large extent by advances in microscope and detector technology. Here, we review some of the complementary technical improvements that are helping sustain the cryo-EM revolution. We highlight advances in image processing that permit high resolution structure determination even in the presence of structural and conformational heterogeneity. We also review selected examples where biochemical strategies for membrane protein stabilization facilitate cryo-EM structure determination, and discuss emerging approaches for further improving the preparation of reliable plunge-frozen specimens.
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页码:71 / 78
页数:8
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