Center for Structural Biology, Vlaams Instituut voor Biotechnologie, Pleinlaan 2, 1050 Brussels, Belgium.
Acta Crystallogr D Struct Biol. 2021 May 1;77(Pt 5):555-564. doi: 10.1107/S2059798321002151. Epub 2021 Apr 14.
Single-particle cryogenic electron microscopy has recently become a major method for determining the structures of proteins and protein complexes. This has markedly increased the demand for throughput of high-resolution electron microscopes, which are required to produce high-resolution images at high rates. An increase in data-collection throughput can be achieved by using large beam-image shifts combined with off-axis coma correction, enabling the acquisition of multiple images from a large area of the EM grid without moving the microscope stage. Here, the optical properties of the JEOL CRYO ARM 300 electron microscope equipped with a K3 camera were characterized under off-axis illumination conditions. It is shown that efficient coma correction can be achieved for beam-image shifts with an amplitude of at least 10 µm, enabling a routine throughput for data collection of between 6000 and 9000 images per day. Use of the benchmark for the rapid data-collection procedure (with beam-image shifts of up to 7 µm) on apoferritin resulted in a reconstruction at a resolution of 1.7 Å. This demonstrates that the rapid automated acquisition of high-resolution micrographs is possible using a CRYO ARM 300.
单颗粒低温电子显微镜技术最近已成为确定蛋白质和蛋白质复合物结构的主要方法。这显著增加了高通量高分辨率电子显微镜的需求,以高速率产生高分辨率图像。通过使用大束流像移并结合离轴彗差校正,可以提高数据采集通量,从而在不移动显微镜载物台的情况下从 EM 栅格的大面积采集多个图像。本文在离轴照明条件下对配备 K3 相机的 JEOL CRYO ARM 300 电子显微镜的光学性能进行了表征。结果表明,对于幅度至少为 10 µm 的束流像移,可以实现有效的彗差校正,从而使每天的数据采集通量达到 6000 到 9000 张图像之间。在脱铁蛋白上使用基准快速数据采集程序(束流像移达 7 µm),得到了分辨率为 1.7 Å 的重构结果。这表明使用 CRYO ARM 300 可以实现高分辨率显微照片的快速自动采集。