Biozentrum, University of Basel, Basel, Switzerland.
Methods Mol Biol. 2020;2127:275-282. doi: 10.1007/978-1-0716-0373-4_18.
The ongoing development of single-particle cryo-electron microscopy (cryo-EM) is leading to fast data acquisition, data processing, and protein structure elucidation. Quick and reliable methods to go from protein purification and optimization to grid preparation will significantly improve the reach and power of cryo-EM. Such methods would particularly constitute a tremendous advantage in structural biology of membrane proteins, whose published structures stay still far behind the number of soluble protein structures. Here we describe a fast, low-cost, and user-friendly method for the purification and cryo-EM analysis of a recombinant membrane protein. This method minimizes the amount of starting material and manipulation steps needed to go from purification to grid preparation, and could potentially be expanded to other membrane protein purification systems for its direct application in structure determination by single-particle cryo-EM.
单颗粒冷冻电子显微镜(cryo-EM)的持续发展正在推动数据采集、处理和蛋白质结构解析的快速发展。从蛋白质纯化和优化到网格制备的快速可靠方法将极大地提高 cryo-EM 的应用范围和能力。对于膜蛋白的结构生物学来说,这些方法尤其具有巨大的优势,因为已经发表的膜蛋白结构数量仍然远远落后于可溶性蛋白结构的数量。在这里,我们描述了一种快速、低成本、用户友好的方法,用于重组膜蛋白的纯化和 cryo-EM 分析。该方法最大限度地减少了从纯化到网格制备所需的起始材料和操作步骤的数量,并可能扩展到其他膜蛋白纯化系统,以便直接应用于单颗粒 cryo-EM 确定结构。