Single Particle Cryo-Electron Microscopy: From Sample to Structure

被引:5
作者
White, Joshua B. R. [1 ]
Maskell, Daniel P. [1 ]
Howe, Andrew [2 ]
Harrow, Martin [2 ]
Clare, Daniel K. [2 ]
Siebert, C. Alistair [2 ]
Hesketh, Emma L. [1 ]
Thompson, Rebecca F. [1 ]
机构
[1] Univ Leeds, Astbury Ctr Struct Mol Biol, Sch Mol & Cellular Biol, Faulty Biol Sci, Leeds, W Yorkshire, England
[2] Harwell Sci & Innovat Campus, Diamond Light Source, Didcot, Oxon, England
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2021年 / 171期
基金
英国惠康基金;
关键词
D O I
10.3791/62415
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
Cryo-electron microscopy (cryoEM) is a powerful technique for structure determination of macromolecular complexes, via single particle analysis (SPA). The overall process involves i) vitrifying the specimen in a thin film supported on a cryoEM grid; ii) screening the specimen to assess particle distribution and ice quality; iii) if the grid is suitable, collecting a single particle dataset for analysis; and iv) image processing to yield an EM density map. In this protocol, an overview for each of these steps is provided, with a focus on the variables which a user can modify during the workflow and the troubleshooting of common issues. With remote microscope operation becoming standard in many facilities, variations on imaging protocols to assist users in efficient operation and imaging when physical access to the microscope is limited will be described.
引用
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页数:25
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