| Literature DB >> 30229291 |
Paul Walther1, Andrea Bauer2, Nadia Wenske2, Alberto Catanese3, Débora Garrido3, Marion Schneider4.
Abstract
Scanning transmission electron microscopic (STEM) tomography of high-pressure frozen, freeze-substituted semi-thin sections is one of multiple approaches for three-dimensional recording and visualization of electron microscopic samples. Compared to regular TEM tomography thicker sample sections can be investigated since chromatic aberration due to inelastic scattering is not a limit. The method is ideal to investigate subcellular compartments or organelles such as synapses, mitochondria, or microtubule arrangements. STEM tomography fills the gap between single-particle electron cryo-tomography, and methods that allow investigations of large volumes, such as serial block-face SEM and FIB-SEM. In this article, we discuss technical challenges of the approach and show some applications in cell biology. It is ideal to use a 300-kV electron microscope with a very small convergence angle of the primary beam ("parallel" beam). These instruments are expensive and tomography is rather time consuming, and therefore, access to such a high-end microscope might be difficult. In this article, we demonstrate examples of successful STEM tomography in biology using a more standard 200-kV microscope equipped with a field emission tip.Keywords: Cell biology; Electron microscopy; Freeze substitution; High pressure freezing; STEM tomography; Synapse
Mesh:
Year: 2018 PMID: 30229291 DOI: 10.1007/s00418-018-1727-0
Source DB: PubMed Journal: Histochem Cell Biol ISSN: 0948-6143 Impact factor: 4.304