Literature DB >> 32557536

Advanced cryo-tomography workflow developments - correlative microscopy, milling automation and cryo-lift-out.

Jakub Kuba1, John Mitchels1, MiloŠ Hovorka1, Philipp Erdmann2, LukÁŠ Berka1, Robert Kirmse3, Julia KÖnig3, Jan DE Bock4, Bernhard Goetze5, Alexander Rigort2,5.   

Abstract

Cryo-electron tomography (cryo-ET) is a groundbreaking technology for 3D visualisation and analysis of biomolecules in the context of cellular structures. It allows structural investigations of single proteins as well as their spatial arrangements within the cell. Cryo-tomograms provide a snapshot of the complex, heterogeneous and transient subcellular environment. Due to the excellent structure preservation in amorphous ice, it is possible to study interactions and spatial relationships of proteins in their native state without interference caused by chemical fixatives or contrasting agents. With the introduction of focused ion beam (FIB) technology, the preparation of cellular samples for electron tomography has become much easier and faster. The latest generation of integrated FIB and scanning electron microscopy (SEM) instruments (dual beam microscopes), specifically designed for cryo-applications, provides advances in automation, imaging and the preparation of high-pressure frozen bulk samples using cryo-lift-out technology. In addition, correlative cryo-fluorescence microscopy provides cellular targeting information through integrated software and hardware interfaces. The rapid advances, based on the combination of correlative cryo-microscopy, cryo-FIB and cryo-ET, have already led to a wealth of new insights into cellular processes and provided new 3D image data of the cell. Here we introduce our recent developments within the cryo-tomography workflow, and we discuss the challenges that lie ahead. LAY DESCRIPTION: This article describes our recent developments for the cryo-electron tomography (cryo-ET) workflow. Cryo-ET offers superior structural preservation and provides 3D snapshots of the interior of vitrified cells at molecular resolution. Before a cellular sample can be imaged by cryo-ET, it must be made accessible for transmission electron microscopy. This is achieved by preparing a 200-300 nm thin cryo-lamella from the cellular sample using a cryo-focused ion beam (cryo-FIB) microscope. Cryo-correlative light and electron microscopy (cryo-CLEM) is used within the workflow to guide the cryo-lamella preparation to the cellular areas of interest. We cover a basic introduction of the cryo-ET workflow and show new developments for cryo-CLEM, which facilitate the connection between the cryo-light microscope and the cryo-FIB. Next, we present our progress in cryo-FIB software automation to streamline cryo-lamella preparation. In the final section we demonstrate how the cryo-FIB can be used for 3D imaging and how bulk-frozen cellular samples (obtained by high-pressure freezing) can be processed using the newly developed cryo-lift-out technology.
© 2020 The Authors. Journal of Microscopy published by John Wiley & Sons Ltd on behalf of Royal Microscopical Society.

Entities:  

Keywords:  Cryo-CLEM; FIB/SEM tomography; cryo-ET; cryo-FIB; cryo-FIB/SEM; cryo-LM; cryo-electron; cryo-focused ion beam; cryo-lift-out; electron-tomography; focused ion beam; lift-out; tomography workflow

Mesh:

Year:  2020        PMID: 32557536     DOI: 10.1111/jmi.12939

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


  9 in total

1.  The In Situ Structure of Parkinson's Disease-Linked LRRK2.

Authors:  Reika Watanabe; Robert Buschauer; Jan Böhning; Martina Audagnotto; Keren Lasker; Tsan-Wen Lu; Daniela Boassa; Susan Taylor; Elizabeth Villa
Journal:  Cell       Date:  2020-08-11       Impact factor: 41.582

2.  A modular platform for automated cryo-FIB workflows.

Authors:  Sven Klumpe; Herman Kh Fung; Sara K Goetz; Ievgeniia Zagoriy; Bernhard Hampoelz; Xiaojie Zhang; Philipp S Erdmann; Janina Baumbach; Christoph W Müller; Martin Beck; Jürgen M Plitzko; Julia Mahamid
Journal:  Elife       Date:  2021-12-24       Impact factor: 8.140

3.  CorRelator: Interactive software for real-time high precision cryo-correlative light and electron microscopy.

Authors:  Jie E Yang; Matthew R Larson; Bryan S Sibert; Samantha Shrum; Elizabeth R Wright
Journal:  J Struct Biol       Date:  2021-02-18       Impact factor: 3.234

4.  How advances in cryo-electron tomography have contributed to our current view of bacterial cell biology.

Authors:  Janine Liedtke; Jamie S Depelteau; Ariane Briegel
Journal:  J Struct Biol X       Date:  2022-02-26

5.  Waffle Method: A general and flexible approach for improving throughput in FIB-milling.

Authors:  Ashleigh M Raczkowski; Oleg Klykov; Pattana Jaroenlak; Daija Bobe; Kotaro Kelley; Mykhailo Kopylov; Edward T Eng; Gira Bhabha; Clinton S Potter; Bridget Carragher; Alex J Noble
Journal:  Nat Commun       Date:  2022-04-06       Impact factor: 14.919

Review 6.  Quantitative Cryo-Electron Tomography.

Authors:  Paula P Navarro
Journal:  Front Mol Biosci       Date:  2022-07-06

Review 7.  Recent Advances in Single-Particle Electron Microscopic Analysis of Autophagy Degradation Machinery.

Authors:  Yiu Wing Sunny Cheung; Sung-Eun Nam; Calvin K Yip
Journal:  Int J Mol Sci       Date:  2020-10-28       Impact factor: 5.923

8.  Cryo-FIB preparation of whole cells and tissue for cryo-TEM: use of high-pressure frozen specimens in tubes and planchets.

Authors:  D A M DE Winter; C Hsieh; M Marko; M F Hayles
Journal:  J Microsc       Date:  2020-07-28       Impact factor: 1.758

9.  An introduction to cryo-FIB-SEM cross-sectioning of frozen, hydrated Life Science samples.

Authors:  M F Hayles; D A M DE Winter
Journal:  J Microsc       Date:  2020-08-24       Impact factor: 1.758

  9 in total

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