Cookies Disclaimer

OK Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

Super-resolution microscopy

Super-resolution microscopy allows to visualize structures in cells that were previously inaccessible. It is progressing at an amazing pace, thereby opening up entire new fields in biology. We use various super-resolution modalities including STED, RESOLFT and GSDIM microscopy, each of them exhibiting different strengths. For example, RESOLFT is especially suited for the imaging of living cells and STED for the fast recording of small areas. A major focus of our research is on the nanoscale architecture and dynamics of mitochondria. We also investigate new labelling strategies and are especially interested in the analysis and development of new fluorescent proteins for RESOLFT super-resolution microscopy.

References

Sahl, S.J., Hell, S.W. & Jakobs, S. : "Fluorescence nanoscopy in cell biology"
Nature Reviews Molecular Biology 18685-701, DOI 10.1038/nrm.2017.71Details

Danzl, J.G., Sidenstein, S.C., Gregor, C., Urban, N.T., Ilgen, P., Jakobs, S., Hell, S.W.: "Coordinate-targeted fluorescence nanoscopy with multiple off states"
Nature Photonics 10 (2), 122-128, DOI 10.1038/nphoton.2015.266Details

Jakobs, S., and Wurm, C.A.: "Super-resolution microscopy of mitochondria"
Curr. Opin. Chem. Biol. 20, 9-15, DOI 10.1016/j.cbpa.2014.03.019Details

Klar, T.A.,Jakobs, S.,Dyba, M.,Egner, A. and Hell, S.W.: "Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission"
PNAS 97 (15), 8206-8210. DOI 10.1073/pnas.97.15.8206Details