4.4 Article

MAVIS: An integrated system for live microscopy and vitrification

Journal

ULTRAMICROSCOPY
Volume 143, Issue -, Pages 67-76

Publisher

ELSEVIER
DOI: 10.1016/j.ultramic.2013.10.007

Keywords

Electron microscopy; Light microscopy; Correlative microscopy; Cryo-microscopy

Categories

Funding

  1. Dutch Cyttron II project - Netherlands Smart Mix grant [FES 2009]
  2. NIMIC partner organizations through NIMIC, a public-private program

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Cryo-elearon microscopy of vitrified biological samples can provide three-dimensional reconstructions of macromolecules and organelles within bacteria and cells at nanometer scale resolution, even in native conditions. Localization of specific structures and imaging of cellular dynamics in cellular cryo-electron microscopy is limited by (i) the use of cryo-rixation to preserve cellular structures, (ii) the restricted availability of electron dense markers to label molecules inside cells and (iii) the inherent low contrast of cryo electron microscopy. These limitations can be mitigated to a large extend by correlative light and electron microscopy, where the sample is imaged by both light and electron microscopy. Here we present a Microscopy and Vitrification Integrated System (MAVIS) that combines a light microscope with a plunger to vitrify thin specimens. MAVIS provides the capability for fluorescence light microscopic imaging of living cells and bacteria that are adhered to an electron microscopy grid and subsequent vitrification within a time frame of seconds. The instrument allows targeting of dynamic biological events in time and space by fluorescence microscopy for subsequent cryo light and electron microscopy. Here we describe the design and performance of the MAVIS. illustrated with biological examples. (C) 2013 Elsevier B.V. All rights reserved.

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