Grassucci Robert A, Taylor Derek J, Frank Joachim
Howard Hughes Medical Institute, Department of Biochemistry and Molecular Biophysics, Columbia University College of Physicians and Surgeons, 630 West 168th Street, New York, New York 10032, USA.
Nat Protoc. 2007;2(12):3239-46. doi: 10.1038/nprot.2007.452.
This protocol describes the preparation of frozen-hydrated single-particle specimens of macromolecular complexes. First, it describes how to create a grid surface coated with holey carbon by first inducing holes in a Formvar film to act as a template for the holey carbon that is stable under cryo-electron microscopy (cryo-EM) conditions and is sample-friendly. The protocol then describes the steps required to deposit the homogeneous sample on the grid and to plunge-freeze the grid into liquid ethane at the temperature of liquid nitrogen, so that it is suitable for cryo-EM visualization. It takes 4-5 h to make several hundred holey carbon grids and about 1 h to make the frozen-hydrated grids. The time required for sample purification varies from hours to days, depending on the sample and the specific procedure required. A companion protocol details how to collect cryo-EM data using an FEI Tecnai transmission electron microscope that can subsequently be processed to obtain a three-dimensional reconstruction of the macromolecular complex.
本方案描述了大分子复合物冷冻水合单颗粒标本的制备方法。首先,它描述了如何通过在福尔马林膜上诱导出孔来创建覆盖有孔碳的网格表面,这些孔作为孔碳的模板,在低温电子显微镜(cryo-EM)条件下稳定且对样品友好。该方案接着描述了将均匀样品沉积在网格上并在液氮温度下将网格投入液氮中骤冷的步骤,使其适用于低温电子显微镜观察。制作数百个有孔碳网格需要4 - 5小时,制作冷冻水合网格约需1小时。样品纯化所需时间从数小时到数天不等,具体取决于样品和所需的特定程序。一个配套方案详细介绍了如何使用FEI Tecnai透射电子显微镜收集低温电子显微镜数据,随后可对这些数据进行处理以获得大分子复合物的三维重建。