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  Optimized cryo-focused ion beam sample preparation aimed at in situ structural studies of membrane proteins

Schaffer, M., Mahamid, J., Engel, B. D., Laugks, T., Baumeister, W., & Plitzko, J. M. (2017). Optimized cryo-focused ion beam sample preparation aimed at in situ structural studies of membrane proteins. Journal of Structural Biology, 197(2), 73-82. doi:10.1016/j.jsb.2016.07.010.

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 Urheber:
Schaffer, Miroslava1, Autor           
Mahamid, Julia1, Autor           
Engel, Benjamin D.1, Autor           
Laugks, Tim1, Autor           
Baumeister, Wolfgang1, Autor           
Plitzko, Jürgen M.1, Autor           
Affiliations:
1Baumeister, Wolfgang / Molecular Structural Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565142              

Inhalt

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Schlagwörter: TRANSMISSION ELECTRON-MICROSCOPY; CRYOELECTRON TOMOGRAPHY; EUKARYOTIC CELLS; ATP SYNTHASE; PHASE PLATE; COMPLEX; CHLAMYDOMONAS; ARCHITECTURE; SPECIMENS; FIBBiochemistry & Molecular Biology; Biophysics; Cell Biology; Cryo-FIB; Sample preparation; Cryo-ET; Volta phase plate; In situ;
 Zusammenfassung: While cryo-electron tomography (cryo-ET) can reveal biological structures in their native state within the cellular environment, it requires the production of high-quality frozen-hydrated sections that are thinner than 300 nm. Sample requirements are even more stringent for the visualization of membrane-bound protein complexes within dense cellular regions. Focused ion beam (FIB) sample preparation for transmission electron microscopy (TEM) is a well-established technique in material science, but there are only few examples of biological samples exhibiting sufficient quality for high-resolution in situ investigation by cryo-ET. In this work, we present a comprehensive description of a cryo-sample preparation workflow incorporating additional conductive-coating procedures. These coating steps eliminate the adverse effects of sample charging on imaging with the Volta phase plate, allowing data acquisition with improved contrast. We discuss optimized FIB milling strategies adapted from material science and each critical step required to produce homogeneously thin, non-charging FIB lamellas that make large areas of unperturbed HeLa and Chlamydomonas cells accessible for cryo-ET at molecular resolution. (C) 2016 Elsevier Inc. All rights reserved.

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Sprache(n): eng - English
 Datum: 2016-07-192017-02
 Publikationsstatus: Erschienen
 Seiten: 10
 Ort, Verlag, Ausgabe: -
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 Art der Begutachtung: -
 Identifikatoren: ISI: 000393268200002
DOI: 10.1016/j.jsb.2016.07.010
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Projektname : ERC-2012-SyG_318987-ToPAG
Grant ID : 318987
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Titel: Journal of Structural Biology
  Kurztitel : J. Struct. Biol.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Orlando, Fla. : Academic Press
Seiten: - Band / Heft: 197 (2) Artikelnummer: - Start- / Endseite: 73 - 82 Identifikator: ISSN: 1047-8477
CoNE: https://pure.mpg.de/cone/journals/resource/954922650160