Literature DB >> 18445162

Moving EM: the Rapid Transfer System as a new tool for correlative light and electron microscopy and high throughput for high-pressure freezing.

P Verkade1.   

Abstract

In this paper, the Rapid Transfer System (RTS), an attachment to the Leica EMPACT2 high-pressure freezer, is described as a new tool for special applications within the cryofixation field. The RTS is an automated system that allows for fast processing of samples (<5 s) that make it possible for the first time to use high-pressure freezing in combination with high time resolution correlative light and electron microscopy. In addition, with a working cycle of 30 s this rapid turn over time allows one to acquire more samples of biopsy material before it deteriorates than with other HPF machines with longer cycle times. With the use of the RTS it was possible to obtain three samples each of four different tissues in 6 min. Together with the finding that 90% of samples of cells grown on sapphire discs were well frozen, the RTS was both fast and reliable. Most important, together with other newly developed accessories, the RTS made it possible to capture specific events occurring live in the cell as observed by light microscopy, to cryofix that sample/event within 4 s, and then to analyze that event at high resolution in the electron microscope with excellent preservation of ultra-structure. These developments should give us the tools to unravel intracellular processes that can be observed by live cell imaging but are too rare or fast to be picked up by routine EM methods or where the history of a structure is necessary to be able to discern its nature.

Mesh:

Year:  2008        PMID: 18445162     DOI: 10.1111/j.1365-2818.2008.01989.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  45 in total

Review 1.  The use of markers for correlative light electron microscopy.

Authors:  Edward Brown; Paul Verkade
Journal:  Protoplasma       Date:  2010-06-05       Impact factor: 3.356

2.  A method for preserving ultrastructural properties of mitotic cells for subsequent immunogold labeling using low-temperature embedding in LR White resin.

Authors:  Margarita Sobol; Jana Nebesářová; Pavel Hozák
Journal:  Histochem Cell Biol       Date:  2010-12-14       Impact factor: 4.304

3.  Intracellular membrane traffic at high resolution.

Authors:  Jan R T van Weering; Edward Brown; Thomas H Sharp; Judith Mantell; Peter J Cullen; Paul Verkade
Journal:  Methods Cell Biol       Date:  2010       Impact factor: 1.441

Review 4.  Out with the old and in with the new: rapid specimen preparation procedures for electron microscopy of sectioned biological material.

Authors:  Kent L McDonald
Journal:  Protoplasma       Date:  2013-11-21       Impact factor: 3.356

Review 5.  Advanced correlative light/electron microscopy: current methods and new developments using Tokuyasu cryosections.

Authors:  Katia Cortese; Alberto Diaspro; Carlo Tacchetti
Journal:  J Histochem Cytochem       Date:  2009-08-03       Impact factor: 2.479

Review 6.  Electron microscopy of high pressure frozen samples: bridging the gap between cellular ultrastructure and atomic resolution.

Authors:  Daniel Studer; Bruno M Humbel; Matthias Chiquet
Journal:  Histochem Cell Biol       Date:  2008-09-16       Impact factor: 4.304

7.  Towards native-state imaging in biological context in the electron microscope.

Authors:  Anne E Weston; Hannah E J Armer; Lucy M Collinson
Journal:  J Chem Biol       Date:  2009-11-15

8.  Substrate Inhibition of VanA by d-Alanine Reduces Vancomycin Resistance in a VanX-Dependent Manner.

Authors:  Lizah T van der Aart; Nicole Lemmens; Willem J van Wamel; Gilles P van Wezel
Journal:  Antimicrob Agents Chemother       Date:  2016-07-22       Impact factor: 5.191

9.  Imaging three-dimensional tissue architectures by focused ion beam scanning electron microscopy.

Authors:  Andrew J Bushby; Kenneth M Y P'ng; Robert D Young; Christian Pinali; Carlo Knupp; Andrew J Quantock
Journal:  Nat Protoc       Date:  2011-05-26       Impact factor: 13.491

10.  Fine structure of the "PcG body" in human U-2 OS cells established by correlative light-electron microscopy.

Authors:  Jana Smigová; Pavel Juda; Dušan Cmarko; Ivan Raška
Journal:  Nucleus       Date:  2011 May-Jun       Impact factor: 4.197

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