Agitation Modules: Flexible Means to Accelerate Automated Freeze Substitution

Author:

Reipert Siegfried1,Goldammer Helmuth1,Richardson Christine2ORCID,Goldberg Martin W.2,Hawkins Timothy J.2,Hollergschwandtner Elena1,Kaufmann Walter A.3,Antreich Sebastian1,Stierhof York-Dieter4

Affiliation:

1. Core Facility Cell Imaging and Ultrastructure Research, University of Vienna, Vienna, Austria

2. Department of Biosciences, Durham University, Durham, United Kingdom

3. Electron Microscopy Facility, Institute of Science and Technology Austria, Klosterneuburg, Austria

4. Center for Plant Molecular Biology (ZMBP), Microscopy, University of Tübingen, Tübingen, Germany

Abstract

For ultrafast fixation of biological samples to avoid artifacts, high-pressure freezing (HPF) followed by freeze substitution (FS) is preferred over chemical fixation at room temperature. After HPF, samples are maintained at low temperature during dehydration and fixation, while avoiding damaging recrystallization. This is a notoriously slow process. McDonald and Webb demonstrated, in 2011, that sample agitation during FS dramatically reduces the necessary time. Then, in 2015, we (H.G. and S.R.) introduced an agitation module into the cryochamber of an automated FS unit and demonstrated that the preparation of algae could be shortened from days to a couple of hours. We argued that variability in the processing, reproducibility, and safety issues are better addressed using automated FS units. For dissemination, we started low-cost manufacturing of agitation modules for two of the most widely used FS units, the Automatic Freeze Substitution Systems, AFS(1) and AFS2, from Leica Microsystems, using three dimensional (3D)-printing of the major components. To test them, several labs independently used the modules on a wide variety of specimens that had previously been processed by manual agitation, or without agitation. We demonstrate that automated processing with sample agitation saves time, increases flexibility with respect to sample requirements and protocols, and produces data of at least as good quality as other approaches.

Funder

Deutsche Forschungsgemeinschaft

Biotechnology and Biological Sciences Research Council, UK

Austria Wirtschaftsservice

Publisher

SAGE Publications

Subject

Histology,Anatomy

Reference55 articles.

1. Freeze-Substitution and Freeze-Drying

2. Humbel BM. Freeze substitution. In: Cavalier A, Spehner D, Humbel BM, editors. Hand book of cryo-preparation methods for electron microscopy. Boca Raton: CRC Press; 2009. p. 319–41.

3. Cavalier A, Spehner D, Humbel BM. Handbook of cryo-preparation methods for electron microscopy. Boca Raton: CRC Press; 2009.

4. Enhanced resolution of membranes in cultured cells by cryoimmobilization and freeze-substitution

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