Wide-field subdiffraction RESOLFT microscopy using fluorescent protein photoswitching
Version of Record online: 29 JAN 2007
Copyright © 2007 Wiley-Liss, Inc.
Microscopy Research and Technique
Volume 70, Issue 3, pages 269–280, March 2007
How to Cite
A. Schwentker, M., Bock, H., Hofmann, M., Jakobs, S., Bewersdorf, J., Eggeling, C. and Hell, S. W. (2007), Wide-field subdiffraction RESOLFT microscopy using fluorescent protein photoswitching. Microsc. Res. Tech., 70: 269–280. doi: 10.1002/jemt.20443
- Issue online: 22 FEB 2007
- Version of Record online: 29 JAN 2007
- Manuscript Accepted: 10 DEC 2006
- Manuscript Received: 15 NOV 2006
- European Union (New and Emerging Science and Technology-SPOTLITE)
- fluorescence microscopy;
- fluorescent proteins;
Subdiffraction fluorescence imaging is presented in a parallelized wide-field arrangement exploiting the principle of reversible saturable/switchable optical transitions (RESOLFT). The diffraction barrier is overcome by photoswitching ensembles of the label protein asFP595 between a nonfluorescent off- and a fluorescent on-state. Relying on ultralow continuous-wave intensities, reversible protein switching facilitates parallelized fast image acquisition. The RESOLFT principle is implemented by illuminating with intensity distributions featuring zero intensity lines that are further apart than the conventional Abbe resolution limit. The subdiffraction resolution is verified by recording live Escherichia coli bacteria labeled with asFP595. The obtained resolution of 50 nm (≈λ/12) is limited only by the spectroscopic properties of the proteins and the imperfections of the optical implementation, but not on principle grounds. Microsc. Res. Tech., 2007. © 2007 Wiley-Liss, Inc.