Literature DB >> 22264536

Correlative light-electron microscopy a potent tool for the imaging of rare or unique cellular and tissue events and structures.

Alexander A Mironov1, Galina V Beznoussenko.   

Abstract

In biology, light microscopy (LM) is usually used to study phenomena at a global scale and to look for unique or rare events, and it also provides an opportunity for live imaging, while the forte of electron microscopy (EM) is the high resolution. Observation of living cells under EM is still impossible. Traditionally, LM and EM observations are carried out in different populations of cells/tissues. The advent of true correlative light-electron microscopy (CLEM) has allowed high-resolution imaging by EM of the very same structure observed by LM. This chapter describes imaging with the help of CLEM. The guidelines presented herein enable researchers to analyze structure of organelles and in particular rare events captured by low-resolution imaging of a population or transient events captured by live imaging can now also be studied at high resolution by EM.
Copyright © 2012 Elsevier Inc. All rights reserved.

Mesh:

Year:  2012        PMID: 22264536     DOI: 10.1016/B978-0-12-391857-4.00010-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  9 in total

Review 1.  The complex ultrastructure of the endolysosomal system.

Authors:  Judith Klumperman; Graça Raposo
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-05-22       Impact factor: 10.005

2.  Correlative scanning-transmission electron microscopy reveals that a chimeric flavivirus is released as individual particles in secretory vesicles.

Authors:  Julien Burlaud-Gaillard; Caroline Sellin; Sonia Georgeault; Rustem Uzbekov; Claude Lebos; Jean-Marc Guillaume; Philippe Roingeard
Journal:  PLoS One       Date:  2014-03-28       Impact factor: 3.240

3.  Coupling of vesicle tethering and Rab binding is required for in vivo functionality of the golgin GMAP-210.

Authors:  Keisuke Sato; Peristera Roboti; Alexander A Mironov; Martin Lowe
Journal:  Mol Biol Cell       Date:  2014-12-03       Impact factor: 4.138

4.  Towards the imaging of Weibel-Palade body biogenesis by serial block face-scanning electron microscopy.

Authors:  M J Mourik; F G A Faas; H Zimmermann; J Eikenboom; A J Koster
Journal:  J Microsc       Date:  2015-01-23       Impact factor: 1.758

5.  X-ray ptychographic and fluorescence microscopy of frozen-hydrated cells using continuous scanning.

Authors:  Junjing Deng; David J Vine; Si Chen; Qiaoling Jin; Youssef S G Nashed; Tom Peterka; Stefan Vogt; Chris Jacobsen
Journal:  Sci Rep       Date:  2017-03-27       Impact factor: 4.379

6.  Fluorescent and Electron-Dense Green Color Emitting Nanodiamonds for Single-Cell Correlative Microscopy.

Authors:  Neeraj Prabhakar; Markus Peurla; Olga Shenderova; Jessica M Rosenholm
Journal:  Molecules       Date:  2020-12-13       Impact factor: 4.411

7.  ATR mediates a checkpoint at the nuclear envelope in response to mechanical stress.

Authors:  Amit Kumar; Michele Mazzanti; Martin Mistrik; Martin Kosar; Galina V Beznoussenko; Alexandre A Mironov; Massimiliano Garrè; Dario Parazzoli; G V Shivashankar; Giorgio Scita; Jiri Bartek; Marco Foiani
Journal:  Cell       Date:  2014-07-31       Impact factor: 41.582

8.  Correlative near-infrared light and cathodoluminescence microscopy using Y2O3:Ln, Yb (Ln = Tm, Er) nanophosphors for multiscale, multicolour bioimaging.

Authors:  S Fukushima; T Furukawa; H Niioka; M Ichimiya; T Sannomiya; N Tanaka; D Onoshima; H Yukawa; Y Baba; M Ashida; J Miyake; T Araki; M Hashimoto
Journal:  Sci Rep       Date:  2016-05-17       Impact factor: 4.379

9.  Direct mineralogical imaging of economic ore and rock samples with multi-modal nonlinear optical microscopy.

Authors:  Mung-Chung Kao; Adrian F Pegoraro; David M Kingston; Albert Stolow; Wen-Chuan Kuo; Patrick H J Mercier; Ankur Gogoi; Fu-Jen Kao; Andrew Ridsdale
Journal:  Sci Rep       Date:  2018-11-16       Impact factor: 4.379

  9 in total

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