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  Cryo-electron tomography-the cell biology that came in from the cold

Wagner, J., Schaffer, M., & Fernandez-Busnadiego, R. (2017). Cryo-electron tomography-the cell biology that came in from the cold. FEBS Letters, 591(17), 2520-2533. doi:10.1002/1873-3468.12757.

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 Urheber:
Wagner, Jonathan1, Autor           
Schaffer, Miroslava1, Autor           
Fernandez-Busnadiego, Ruben1, Autor           
Affiliations:
1Baumeister, Wolfgang / Molecular Structural Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565142              

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Schlagwörter: TRANSMISSION ELECTRON-MICROSCOPY; TRIPEPTIDYL-PEPTIDASE-II; CRYO-LIGHT MICROSCOPY; BEAM-INDUCED MOTION; MEAN FREE-PATH; IN-SITU; MOLECULAR ARCHITECTURE; STRUCTURAL-ANALYSIS; PHASE-CONTRAST; MULTICELLULAR ORGANISMSBiochemistry & Molecular Biology; Biophysics; Cell Biology; Cryo-EM; cryo-FIB; protein aggregation;
 Zusammenfassung: Cryo-electron tomography (cryo-ET) provides high-resolution 3D views into cells pristinely preserved by vitrification. Recent technical advances such as direct electron detectors, the Volta phase plate and cryo-focused ion beam milling have dramatically pushed image quality and expanded the range of cryo-ET applications. Cryo-ET not only allows mapping the positions and interactions of macromolecules within their intact cellular context, but can also reveal their in situ structure at increasing resolution. Here, we review how recent work using cutting-edge cryo-ET technologies is starting to provide fresh views into different aspects of cellular biology at an unprecedented level of detail. We anticipate that these developments will soon make cryo-ET a fundamental technique in cell biology.

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Sprache(n): eng - English
 Datum: 2017
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 000409313500003
DOI: 10.1002/1873-3468.12757
 Art des Abschluß: -

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Projektinformation

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Projektname : FP7 GA ERC-2012-SyG_318987–ToPAG
Grant ID : 318987
Förderprogramm : Funding Programme 7 (FP7)
Förderorganisation : European Commission (EC)

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Titel: FEBS Letters
  Andere : FEBS Lett.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Amsterdam : Elsevier
Seiten: SI: Jerusalem Special Issue Band / Heft: 591 (17) Artikelnummer: - Start- / Endseite: 2520 - 2533 Identifikator: ISSN: 0014-5793
CoNE: https://pure.mpg.de/cone/journals/resource/954925399501