Literature DB >> 24269483

A new tool based on two micromanipulators facilitates the handling of ultrathin cryosection ribbons.

Daniel Studer1, Alycia Klein1, Ioan Iacovache1, Helmut Gnaegi2, Benoît Zuber3.   

Abstract

A close to native structure of bulk biological specimens can be imaged by cryo-electron microscopy of vitreous sections (CEMOVIS). In some cases structural information can be combined with X-ray data leading to atomic resolution in situ. However, CEMOVIS is not routinely used. The two critical steps consist of producing a frozen section ribbon of a few millimeters in length and transferring the ribbon onto an electron microscopy grid. During these steps, the first sections of the ribbon are wrapped around an eyelash (unwrapping is frequent). When a ribbon is sufficiently attached to the eyelash, the operator must guide the nascent ribbon. Steady hands are required. Shaking or overstretching may break the ribbon. In turn, the ribbon immediately wraps around itself or flies away and thereby becomes unusable. Micromanipulators for eyelashes and grids as well as ionizers to attach section ribbons to grids were proposed. The rate of successful ribbon collection, however, remained low for most operators. Here we present a setup composed of two micromanipulators. One of the micromanipulators guides an electrically conductive fiber to which the ribbon sticks with unprecedented efficiency in comparison to a not conductive eyelash. The second micromanipulator positions the grid beneath the newly formed section ribbon and with the help of an ionizer the ribbon is attached to the grid. Although manipulations are greatly facilitated, sectioning artifacts remain but the likelihood to investigate high quality sections is significantly increased due to the large number of sections that can be produced with the reported tool.
Copyright © 2013 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cryo-electron microscopy; Cryosectioning; Electron microscopy; Frozen-hydrated sections; High pressure freezing; Micromanipulation; Ultramicrotomy

Mesh:

Year:  2013        PMID: 24269483     DOI: 10.1016/j.jsb.2013.11.005

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  8 in total

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Authors:  Felix R Wagner; Reika Watanabe; Ruud Schampers; Digvijay Singh; Hans Persoon; Miroslava Schaffer; Peter Fruhstorfer; Jürgen Plitzko; Elizabeth Villa
Journal:  Nat Protoc       Date:  2020-05-13       Impact factor: 13.491

2.  Electron microscopy for imaging organelles in plants and algae.

Authors:  Ethan Weiner; Justine M Pinskey; Daniela Nicastro; Marisa S Otegui
Journal:  Plant Physiol       Date:  2022-02-04       Impact factor: 8.005

3.  Serial Cryomicrotomy of Saccharomyces cerevisiae for Serial Electron Cryotomography.

Authors:  Cai Tong Ng; Mark S Ladinsky; Lu Gan
Journal:  Bio Protoc       Date:  2020-11-20

4.  Cryo-ET detects bundled triple helices but not ladders in meiotic budding yeast.

Authors:  Olivia X Ma; Wen Guan Chong; Joy K E Lee; Shujun Cai; C Alistair Siebert; Andrew Howe; Peijun Zhang; Jian Shi; Uttam Surana; Lu Gan
Journal:  PLoS One       Date:  2022-04-14       Impact factor: 3.752

Review 5.  Electron microscopy for ultrastructural analysis and protein localization in Saccharomyces cerevisiae.

Authors:  Andri Frankl; Muriel Mari; Fulvio Reggiori
Journal:  Microb Cell       Date:  2015-10-12

6.  Electron cryotomography analysis of Dam1C/DASH at the kinetochore-spindle interface in situ.

Authors:  Cai Tong Ng; Li Deng; Chen Chen; Hong Hwa Lim; Jian Shi; Uttam Surana; Lu Gan
Journal:  J Cell Biol       Date:  2018-11-30       Impact factor: 10.539

7.  Investigating eukaryotic cells with cryo-ET.

Authors:  Cai Tong Ng; Lu Gan
Journal:  Mol Biol Cell       Date:  2020-01-15       Impact factor: 4.138

8.  Hierarchical imaging: a new concept for targeted imaging of large volumes from cells to tissues.

Authors:  Irene Wacker; Waldemar Spomer; Andreas Hofmann; Marlene Thaler; Stefan Hillmer; Ulrich Gengenbach; Rasmus R Schröder
Journal:  BMC Cell Biol       Date:  2016-12-12       Impact factor: 4.241

  8 in total

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