Literature DB >> 33367997

Getting Started with In Situ Cryo-Electron Tomography.

Daniel Serwas1, Karen M Davies2,3.   

Abstract

Cryo-electron tomography (cryo-ET) is an extremely powerful tool which is used to image cellular features in their close-to-native environment at a resolution where both protein structure and membrane morphology can be revealed. Compared to conventional electron microscopy methods for biology, cryo-ET does not include the use of potentially artifact generating agents for sample fixation or visualization. Despite its obvious advantages, cryo-ET has not been widely adopted by cell biologists. This might originate from the overwhelming and constantly growing number of complex ways to record and process data as well as the numerous methods available for sample preparation. In this chapter, we will take one step back and guide the reader through the essential steps of sample preparation using mammalian cells, as well as the basic steps involved in data recording and processing. The described protocol will allow the reader to obtain data that can be used for morphological analysis and precise measurements of biological structures in their cellular environment. Furthermore, this data can be used for more elaborate structural analysis by applying further image processing steps like subtomogram averaging, which is required to determine the structure of proteins.

Entities:  

Keywords:  Cell biology; Cellular morphology; Cryo-electron tomography; Mammalian cells; Segmentation; Structural cell biology; Tilt series; Vitrification

Mesh:

Year:  2021        PMID: 33367997     DOI: 10.1007/978-1-0716-0966-8_1

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  32 in total

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Journal:  Trends Cell Biol       Date:  1999-03       Impact factor: 20.808

2.  Macromolecular architecture in eukaryotic cells visualized by cryoelectron tomography.

Authors:  Ohad Medalia; Igor Weber; Achilleas S Frangakis; Daniela Nicastro; Gunther Gerisch; Wolfgang Baumeister
Journal:  Science       Date:  2002-11-08       Impact factor: 47.728

Review 3.  Whatever happened to the 'microtrabecular concept'?

Authors:  John Heuser
Journal:  Biol Cell       Date:  2002-12       Impact factor: 4.458

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Journal:  Am J Anat       Date:  1954-03

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Journal:  Anat Rec       Date:  1952-11

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Authors:  R Grimm; H Singh; R Rachel; D Typke; W Zillig; W Baumeister
Journal:  Biophys J       Date:  1998-02       Impact factor: 4.033

Review 7.  Cryo-electron microscopy of vitrified specimens.

Authors:  J Dubochet; M Adrian; J J Chang; J C Homo; J Lepault; A W McDowall; P Schultz
Journal:  Q Rev Biophys       Date:  1988-05       Impact factor: 5.318

8.  Cryo-electron microscopy of viruses.

Authors:  M Adrian; J Dubochet; J Lepault; A W McDowall
Journal:  Nature       Date:  1984 Mar 1-7       Impact factor: 49.962

9.  A STUDY OF TISSUE CULTURE CELLS BY ELECTRON MICROSCOPY : METHODS AND PRELIMINARY OBSERVATIONS.

Authors:  K R Porter; A Claude; E F Fullam
Journal:  J Exp Med       Date:  1945-03-01       Impact factor: 14.307

Review 10.  Cryo-electron tomography: the challenge of doing structural biology in situ.

Authors:  Vladan Lučič; Alexander Rigort; Wolfgang Baumeister
Journal:  J Cell Biol       Date:  2013-08-05       Impact factor: 10.539

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  1 in total

1.  Mechanistic insights into actin force generation during vesicle formation from cryo-electron tomography.

Authors:  Daniel Serwas; Matthew Akamatsu; Amir Moayed; Karthik Vegesna; Ritvik Vasan; Jennifer M Hill; Johannes Schöneberg; Karen M Davies; Padmini Rangamani; David G Drubin
Journal:  Dev Cell       Date:  2022-05-02       Impact factor: 13.417

  1 in total

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