New hardware and workflows for semi-automated correlative cryo-fluorescence and cryo-electron microscopy/tomography

被引:73
作者
Schorb, Martin [1 ,2 ]
Gaechter, Leander [3 ]
Avinoam, On [1 ]
Sieckmann, Frank [4 ]
Clarke, Maid [1 ]
Bebeacua, Cecilia [1 ,5 ]
Bykov, Yury S. [1 ]
Sonnen, Andreas F. -P. [1 ,6 ]
Lihl, Reinhard [7 ]
Briggs, John A. G. [1 ,5 ,6 ]
机构
[1] European Mol Biol Lab, Struct & Computat Biol Unit, Meyerhofstr 1, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab, Electron Microscopy Core Facil, Meyerhofstr 1, D-69117 Heidelberg, Germany
[3] Leica Microsyst Schweiz AG, Max Schmidheiny Str 201, CH-9435 Heerbrugg, Switzerland
[4] Leica Microsyst GmbH, Friedenspl 3, D-68165 Mannheim, Germany
[5] European Mol Biol Lab, Cell Biol & Biophys Unit, Meyerhofstr 1, D-69117 Heidelberg, Germany
[6] EMBL Univ Klinikum Heidelberg, Mol Med Partnership Unit, Heidelberg, Germany
[7] Leica Mikrosyst GmbH, Hernalser Hauptstr 219, A-1170 Vienna, Austria
关键词
Correlative light and electron microscopy; CrIfo-fluorescence microscopy; Cryo-electron microscopy; Cryo-electron tomography; ELECTRON-MICROSCOPY; LIGHT-MICROSCOPY; STRUCTURAL BIOLOGY; SPATIAL PRECISION; TOMOGRAPHY; CELLS; SUPERRESOLUTION; VISUALIZATION; SENSITIVITY; SECTIONS;
D O I
10.1016/j.jsb.2016.06.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Correlative light and electron microscopy allows features of interest defined by fluorescence signals to be located in an electron micrograph of the same sample. Rare dynamic events or specific objects can be identified, targeted and imaged by electron microscopy or tomography. To combine it with structural studies using cryo-electron microscopy or tomography, fluorescence microscopy must be performed while maintaining the specimen vitrified at liquid-nitrogen temperatures and in a dry environment during imaging and transfer. Here we present instrumentation, software and an experimental workflow that improves the ease of use, throughput and performance of correlated cryo-fluorescence and cryo-electron microscopy. The new cryo-stage incorporates a specially modified high-numerical aperture objective lens and provides a stable and clean imaging environment. It is combined with a transfer shuttle for contamination-free loading of the specimen. Optimized microscope control software allows automated acquisition of the entire specimen area by cryo-fluorescence microscopy. The software also facilitates direct transfer of the fluorescence image and associated coordinates to the cryo-electron microscope for subsequent fluorescence-guided automated imaging. Here we describe these technological developments and present a detailed workflow, which we applied for automated cryo-electron microscopy and tomography of various specimens. (C) 2016 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license.
引用
收藏
页码:83 / 93
页数:11
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