Protocol

Immersion Freezing of Cell Monolayers for Cryo-Electron Tomography

  1. Edit Urban3
  1. 1IMP-IMBA-GMI Electron Microscopy Facility, Institute of Molecular Biotechnology, 1030 Vienna, Austria
  2. 2University of Applied Sciences Wiener Neustadt, 2700 Wiener Neustadt, Austria
  3. 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

    • 4 Corresponding author (guenter.resch{at}imba.oeaw.ac.at).

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