Sample preparation and image registration for correlative cryo-FM and cryo-FIB-SEM of plunge-frozen mammalian cells

被引:0
|
作者
Scher, Nadav [1 ]
Rechav, Katya [2 ]
Paul-Gilloteaux, Perrine [3 ]
Avinoam, Ori [1 ]
机构
[1] Weizmann Inst Sci, Dept Biomol Sci, Rehovot, Israel
[2] Weizmann Inst Sci, Dept Chem Res Support, Rehovot, Israel
[3] Univ Nantes, Struct Federat Rech Francois Bonamy, INSERM, CNRS, Nantes, France
来源
STAR PROTOCOLS | 2022年 / 3卷 / 01期
基金
欧洲研究理事会;
关键词
PLATFORM;
D O I
10.1016/j.xpro.2022.101142
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We recently demonstrated how lipid droplets can serve as in situ fiducials for correlating cryo-fluorescence microscopy (cryo-FM) and cryo-focused ion beam scanning electron microscopy (cryo-FIB-SEM) datasets of mammalian cells grown on grids. Here we describe a step-by-step protocol for correlative cryo-FM and cryo-FIB-SEM, starting from sample preparation of C2C12 cell line, followed by imaging with cryo-FM and cryo-FIB-SEM. Finally, we detail how to perform the 3D-correlation with sub-micron accuracy.For complete details on the use and execution of this profile, please refer to Scher et al. (2021).
引用
收藏
页数:24
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