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Super-Resolution STED and STORM/PALM Microscopy for Brain Imaging

  • Boris Egger
  • Simon G. Sprecher
Chapter
Part of the Progress in Optical Science and Photonics book series (POSP, volume 5)

Abstract

Cellular processes in the brain allow for most complex computations, which in turn provide the basis of any form of behaviour. With the advent of diffraction-unlimited imaging techniques, it is now possible to study processes in neurons with unprecedented subcellular resolution. Based on the illumination and recording techniques, two approaches are dominating super-resolution microscopy: stimulated emission depletion (STED) microscopy, which is based on image scanning, and stochastic optical reconstruction microscopy (STORM)/photoactivated localization microscopy (PALM), which makes use of single-molecule localization. In the last decade, both approaches led to spectacular insight into the nanostructure of various neuronal compartments. We highlight a selection of studies, in which neuronal structures and processes were imaged with super-resolution, including the cytoskeleton of axons, plasticity in dendritic spines as well as molecular arrangements in presynaptic terminals and active zones.

Keywords

STORM STED Microscopy Brain Neurons 

Notes

Acknowledgements

We thank Elisa D’Este, Stefan Hell, Valentin Nägerl, Stephan Sigrist and Xiaowei Zhuang for permission to reproduce their published work. SGS is funded by the European Research Council (ERC-2012-StG 309832-PhotoNaviNet) and the Swiss National Science Foundation (31003A_169993).

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Copyright information

© Springer Nature Singapore Pte Ltd. 2019

Authors and Affiliations

  1. 1.Department of BiologyUniversity of FribourgFribourgSwitzerland

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