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  New hardware and workflows for semi-automated correlative cryo-fluorescence and cryo-electron microscopy/tomography

Schorb, M., Gaechter, L., Avinoam, O., Sieckmann, F., Clarke, M., Bebeacua, C., et al. (2017). New hardware and workflows for semi-automated correlative cryo-fluorescence and cryo-electron microscopy/tomography. Journal of Structural Biology, 197(2), 83-93. doi:10.1016/j.jsb.2016.06.020.

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 Creators:
Schorb, M., Author
Gaechter, L., Author
Avinoam, O., Author
Sieckmann, F., Author
Clarke, M., Author
Bebeacua, C., Author
Bykov, Y. S., Author
Sonnen, A. F. P., Author
Lihl, R., Author
Briggs, John A. G.1, Author           
Affiliations:
1European Molecular Biology Laboratory, External Organizations, ou_3346677              

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Free keywords: Correlative light and electron microscopy CrIfo-fluorescence microscopy Cryo-electron microscopy Cryo-electron tomography electron-microscopy light-microscopy structural biology spatial precision tomography cells superresolution visualization sensitivity sections Biochemistry & Molecular Biology Biophysics Cell Biology
 Abstract: Correlative light and electron microscopy allows features of interest defined by fluorescence signals to be located in an electron micrograph of the same sample. Rare dynamic events or specific objects can be identified, targeted and imaged by electron microscopy or tomography. To combine it with structural studies using cryo-electron microscopy or tomography, fluorescence microscopy must be performed while maintaining the specimen vitrified at liquid-nitrogen temperatures and in a dry environment during imaging and transfer. Here we present instrumentation, software and an experimental workflow that improves the ease of use, throughput and performance of correlated cryo-fluorescence and cryo-electron microscopy. The new cryo-stage incorporates a specially modified high-numerical aperture objective lens and provides a stable and clean imaging environment. It is combined with a transfer shuttle for contamination-free loading of the specimen. Optimized microscope control software allows automated acquisition of the entire specimen area by cryo-fluorescence microscopy. The software also facilitates direct transfer of the fluorescence image and associated coordinates to the cryo-electron microscope for subsequent fluorescence-guided automated imaging. Here we describe these technological developments and present a detailed workflow, which we applied for automated cryo-electron microscopy and tomography of various specimens. (C) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license.

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Language(s): eng - English
 Dates: 2017
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: Other: WOS:000393268200003
DOI: 10.1016/j.jsb.2016.06.020
ISSN: 1047-8477
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Title: Journal of Structural Biology
  Alternative Title : J. Struct. Biol.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 197 (2) Sequence Number: - Start / End Page: 83 - 93 Identifier: -