Structural Biology of Molecular Machines Group, Protein Structure & Function Programme, Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Methods Mol Biol. 2020;2127:227-244. doi: 10.1007/978-1-0716-0373-4_16.
Cryo-electron microscopy (cryo-EM) is a powerful tool for investigating the structure of macromolecules under near-native conditions. Especially in the context of membrane proteins, this technique has allowed researchers to obtain structural information at a previously unattainable level of detail. Specimen preparation remains the bottleneck of most cryo-EM research projects, with membrane proteins representing particularly challenging targets of investigation due to their universal requirement for detergents or other solubilizing agents. Here we describe preparation of negative staining and cryo-EM grids and downstream data collection of membrane proteins in detergent, by far the most common solubilization agent. This protocol outlines a quick and straightforward procedure for screening and determining the structure of a membrane protein of interest under biologically relevant conditions.
冷冻电子显微镜(cryo-EM)是一种强大的工具,可用于在近乎天然的条件下研究大分子的结构。特别是在膜蛋白的情况下,该技术使研究人员能够以前所未有的详细程度获得结构信息。标本制备仍然是大多数 cryo-EM 研究项目的瓶颈,由于膜蛋白普遍需要去污剂或其他增溶剂,因此它们是特别具有挑战性的研究目标。在这里,我们描述了负染色和 cryo-EM 网格的制备,以及去污剂中膜蛋白的下游数据收集,去污剂是迄今为止最常用的增溶剂。该方案概述了一种快速而直接的程序,用于在生物相关条件下筛选和确定感兴趣的膜蛋白的结构。