DocumentCode :
2300502
Title :
Far-field optical nanoscopy
Author :
Hell, Stefan W.
Author_Institution :
Dept. of NanoBiophotonics, Max Planck Inst. for Biophys. Chem., Göttingen, Germany
fYear :
2010
fDate :
7-11 Nov. 2010
Firstpage :
3
Lastpage :
4
Abstract :
In this paper physical concepts that radically break the diffraction barrier in focusing fluorescence microscopy has been discussed. They share a common strategy: exploiting selected molecular transitions of the fluorescent marker to neutralize the limiting role of diffraction. The first viable concept of this kind was Stimulated Emission Depletion (STED) microscopy. In its simplest variant, STED microscopy uses a focused beam for fluorescence excitation, along with a red-shifted doughnut-shaped beam for subsequent quenching of fluorescent molecules by stimulated emission.
Keywords :
fluorescence; molecular biophysics; nanobiotechnology; optical microscopy; proteins; radiation quenching; red shift; stimulated emission; STED microscopy; diffraction barrier; far-field optical nanoscopy; fluorescence excitation; fluorescence microscopy; quenching; red-shifted doughnut-shaped beam; selected molecular transitions; stimulated emission depletion microscopy;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
IEEE Photonics Society, 2010 23rd Annual Meeting of the
Conference_Location :
Denver, CO
ISSN :
-
Print_ISBN :
978-1-4244-5368-9
Electronic_ISBN :
-
Type :
conf
DOI :
10.1109/PHOTONICS.2010.5698725
Filename :
5698725
Link To Document :
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