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The Effect of Electron Beam Irradiation in Environmental Scanning Transmission Electron Microscopy of Whole Cells in Liquid

Published online by Cambridge University Press:  03 May 2016

Justus Hermannsdörfer
Affiliation:
INM – Leibniz Institute for New Materials, 66123 Saarbrücken, Germany
Verena Tinnemann
Affiliation:
INM – Leibniz Institute for New Materials, 66123 Saarbrücken, Germany
Diana B. Peckys
Affiliation:
Department of Biophysics, Saarland University, 66421 Homburg/Saar, Germany
Niels de Jonge*
Affiliation:
INM – Leibniz Institute for New Materials, 66123 Saarbrücken, Germany Department of Physics, University of Saarland, 66123 Saarbrücken, Germany
*
*Corresponding author. niels.dejonge@leibniz-inm.de
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Abstract

Whole cells can be studied in their native liquid environment using electron microscopy, and unique information about the locations and stoichiometry of individual membrane proteins can be obtained from many cells thus taking cell heterogeneity into account. Of key importance for the further development of this microscopy technology is knowledge about the effect of electron beam radiation on the samples under investigation. We used environmental scanning electron microscopy (ESEM) with scanning transmission electron microscopy (STEM) detection to examine the effect of radiation for whole fixed COS7 fibroblasts in liquid. The main observation was the localization of nanoparticle labels attached to epidermal growth factor receptors (EGFRs). It was found that the relative distances between the labels remained mostly unchanged (<1.5%) for electron doses ranging from the undamaged native state at 10 e2 toward 103 e2. This dose range was sufficient to determine the EGFR locations with nanometer resolution and to distinguish between monomers and dimers. Various different forms of radiation damage became visible at higher doses, including severe dislocation, and the dissolution of labels.

Type
Biological Applications
Copyright
Copyright © Microscopy Society of America 2016

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