Max Planck Institute of Biochemistry.
Max Planck Institute of Biochemistry; Max Planck Institute for Biophysics.
J Vis Exp. 2021 Oct 25(176). doi: 10.3791/62886.
Cryo-electron tomography (cryo-ET) has become the method of choice for investigating cellular ultrastructure and molecular complexes in their native, frozen-hydrated state. However, cryo-ET requires that samples are thin enough to not scatter or block the incident electron beam. For thick cellular samples, this can be achieved by cryo-focused ion beam (FIB) milling. This protocol describes how to target specific cellular sites during FIB milling using a 3D-correlative approach, which combines three-dimensional fluorescence microscopy data with information from the FIB-scanning electron microscope. Using this technique, rare cellular events and structures can be targeted with high accuracy and visualized at molecular resolution using cryo-transmission electron microscopy (cryo-TEM).
冷冻电子断层扫描(cryo-ET)已成为研究细胞超微结构和分子复合物在其自然冷冻水合状态下的首选方法。然而,cryo-ET 需要样品足够薄,以避免散射或阻挡入射电子束。对于厚的细胞样品,可以通过冷冻聚焦离子束(FIB)铣削来实现。本方案描述了如何在 FIB 铣削过程中使用 3D 相关方法靶向特定的细胞位点,该方法将三维荧光显微镜数据与 FIB 扫描电子显微镜的信息相结合。使用该技术,可以以高精度靶向罕见的细胞事件和结构,并使用 cryo-传输电子显微镜(cryo-TEM)在分子分辨率下进行可视化。