Combining high‐pressure freezing with pre‐embedding immunogold electron microscopy and tomography |
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| Authors: | Michael W Hess Georg F Vogel Teodor E Yordanov Barbara Witting Karin Gutleben Hannes L Ebner Mariana E G de Araujo Przemyslaw A Filipek Lukas A Huber |
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| Affiliation: | 1. Division of Histology and Embryology, Medical University of Innsbruck, Innsbruck, Austria;2. Division of Cell Biology, Biocenter, Medical University of Innsbruck, Innsbruck, Austria;3. Department of Pediatrics I, Medical University of Innsbruck, Innsbruck, Austria |
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| Abstract: | Immunogold labeling of permeabilized whole‐mount cells or thin‐sectioned material is widely used for the subcellular localization of biomolecules at the high spatial resolution of electron microscopy (EM). Those approaches are well compatible with either 3‐dimensional (3D) reconstruction of organelle morphology and antigen distribution or with rapid cryofixation—but not easily with both at once. We describe here a specimen preparation and labeling protocol for animal cell cultures, which represents a novel blend of specifically adapted versions of established techniques. It combines the virtues of reliably preserved organelle ultrastructure, as trapped by rapid freezing within milliseconds followed by freeze‐substitution and specimen rehydration, with the advantages of robust labeling of intracellular constituents in 3D through means of pre‐embedding NANOGOLD‐silver immunocytochemistry. So obtained thin and semi‐thick epoxy resin sections are suitable for transmission EM imaging, as well as tomographic reconstruction and modeling of labeling patterns in the 3D cellular context.  |
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| Keywords: | 3D reconstruction autometallography cryofixation freeze‐substitution high‐resolution imaging immunoelectron tomography immunolabeling rapid freezing silver enhancement STEM‐tomography |
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