Title :
Towards far-field fluorescence nanoscopy
Author :
Hell, S.W. ; Dyba, M.
Author_Institution :
High Resolution Opt. Microscopy Group, Max-Planck-Inst. fur Biophys. Chem., Gottingen, Germany
Abstract :
Summary form only given. Far-field microscopy has been plagued by the diffraction resolution limit. This is particularly restraining in the case of fluorescence imaging of biological specimens such as live cells. Here we report on the creation spots of excited molecules at the tens of nanometer scale, with focused red light and conventionally focusing optics. The underlying strategy is the engineering of the microscope´s point-spread-function by stimulated emission depletion and interference. Sub-diffraction spots enable for the first time far-field fluorescence microscopy with axial resolution at the scale of 30-50 nm.
Keywords :
biological techniques; cellular biophysics; fluorescence; image resolution; light interference; molecular biophysics; optical focusing; optical microscopy; optical transfer function; stimulated emission; axial resolution; biological specimens; excited molecules; far-field fluorescence nanoscopy; far-field microscopy; fluorescence imaging; focusing optics; light interference; live cells; point-spread-function; stimulated emission depletion; subdiffraction spots; Biomedical optical imaging; Cells (biology); Fluorescence; Focusing; Interference; Microscopy; Nanobioscience; Optical diffraction; Optical imaging; Stimulated emission;
Conference_Titel :
Quantum Electronics and Laser Science, 2003. QELS. Postconference Digest
Conference_Location :
Baltimore, MD, USA
Print_ISBN :
1-55752-749-0
DOI :
10.1109/QELS.2003.237847