Immersion Freezing of Cell Monolayers for Cryo-Electron Tomography
- 1IMP-IMBA-GMI Electron Microscopy Facility, Institute of Molecular Biotechnology, 1030 Vienna, Austria
- 2University of Applied Sciences Wiener Neustadt, 2700 Wiener Neustadt, Austria
- 3Institute of Molecular Biotechnology, 1030 Vienna, Austria
INTRODUCTION
Cryo-transmission electron microscopy (cryo-TEM) is not limited to the visualization of suspended macromolecules in their native hydrated state. It can also be used to elucidate the molecular architecture of peripheral parts of adherent cells: After cultivation of the cells directly on EM grids, they are physically fixed by immersion freezing to yield cells embedded in thin, crystal-free layers of frozen water. Subsequently, specimens can be visualized using cryo-electron tomography (cryo-ET). This protocol outlines the production of protein-coated gold particles as suitable fiducial markers for electron tomography, and how to cultivate cells on grids with a carbon support film. It also describes how to freeze cells to obtain optimal and reproducible results using the Leica EM GP immersion freezer, and how to assess the results.
Footnotes
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↵4 Corresponding author (guenter.resch{at}imba.oeaw.ac.at).
- © 2011 Cold Spring Harbor Laboratory Press










