Passmore L A, Russo C J
MRC Laboratory of Molecular Biology, Cambridge, United Kingdom.
Methods Enzymol. 2016;579:51-86. doi: 10.1016/bs.mie.2016.04.011. Epub 2016 Jun 16.
Imaging a material with electrons at near-atomic resolution requires a thin specimen that is stable in the vacuum of the transmission electron microscope. For biological samples, this comprises a thin layer of frozen aqueous solution containing the biomolecular complex of interest. The process of preparing a high-quality specimen is often the limiting step in the determination of structures by single-particle electron cryomicroscopy (cryo-EM). Here, we describe a systematic approach for going from a purified biomolecular complex in aqueous solution to high-resolution electron micrographs that are suitable for 3D structure determination. This includes a series of protocols for the preparation of vitrified specimens on various supports, including all-gold and graphene. We also describe techniques for troubleshooting when a preparation fails to yield suitable specimens, and common mistakes to avoid during each part of the process. Finally, we include recommendations for obtaining the highest quality micrographs from prepared specimens with current microscope, detector, and support technology.
用电子以近原子分辨率对材料进行成像需要一个在透射电子显微镜的真空中稳定的薄样本。对于生物样本来说,这包括一层含有感兴趣的生物分子复合物的冷冻水溶液薄层。制备高质量样本的过程通常是单颗粒电子冷冻显微镜(冷冻电镜)结构测定中的限制步骤。在这里,我们描述了一种从水溶液中的纯化生物分子复合物到适合三维结构测定的高分辨率电子显微照片的系统方法。这包括一系列在各种支撑物上制备玻璃化样本的方案,包括全金和石墨烯支撑物。我们还描述了制备失败无法得到合适样本时的故障排除技术,以及在过程的每个部分要避免的常见错误。最后,我们给出了利用当前的显微镜、探测器和支撑技术从制备好的样本中获得最高质量显微照片的建议。