Ground-State-Depletion Fluorescence Microscopy provides subdiffraction resolution through triplet state pumping

Stefan Bretschneider, Christian Eggeling, Mariano Bossi, Stefan Hell
  1. Abteilung NanoBiophotonik, Max-Planck-Institut für biophysikalische Chemie

sbretsc [at] gwdg [dot] de

The resolution of optical imaging in conventional far-field microscopy is limited by the diffraction of light. We present fluorescence imaging beyond this barrier by forcing the fluorophore into a non-fluorescent state in the outer region of the focus. As an example this non-fluorescent state is realized by the fluorophore's triplet state. Thus the fluorescence emission in the outer region of the diffraction limited excitation spot is deactivated in a saturated manner, thereby dynamically reducing the effective fluorescence volume down to 50 nm in lateral direction. Increased resolution is shown on sub-diffraction scanning images of different fluorescently stained structures. It is shown that a reversible saturable optical fluorescence transition of a dye molecule can be utilized to achieve optical imaging beyond the diffraction barrier.

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@inproceedings{bretschneider2006a36,
  author     = {Bretschneider, Stefan and Eggeling, Christian and Bossi, Mariano and Hell, Stefan},
  title      = {{Ground-State-Depletion Fluorescence Microscopy provides subdiffraction resolution through triplet state pumping}},
  booktitle  = {DGaO-Proceedings 2006},
  series     = {DGaO-Proceedings},
  eventtitle = {107. Jahrestagung der DGaO},
  eventdate  = {2006-06-07/2006-06-10},
  venue      = {Weingarten},
  publisher  = {Deutsche Gesellschaft für angewandte Optik e.V.},
  year       = {2006},
  pages      = {A36},
  langid     = {english},
  url        = {https://dgao-proceedings.de/paper/107-a36}
}
107. Jahrestagung der DGaO · Weingarten · 2006