Light quenching and fluorescence depolarization of rhodamine B and applications of this phenomenon to biophysics
- 1 January 1994
- journal article
- Published by American Chemical Society (ACS) in The Journal of Physical Chemistry
- Vol. 98 (1), 334-342
- https://doi.org/10.1021/j100052a055
Abstract
The fluorescence intensity of rhodamine B (RhB) was found to display a sublinear dependence on incident power when excited with the focused output of a cavity-dumped dye laser. This effect was found to be proportional to the amplitude of the emission spectrum at the incident wavelength and to be associated with a decrease in the time-zero anisotropy of RhB. The absence of changes in the intensity decay law or rotational correlation time indicates the absence of photochemical processes. These results are consistent with "light quenching" of RhB due to stimulated emission. In viscous solution the extent of depolarization of the emission was found to be in agreement with theoretical expressions which account for photoselective light quenching and for spatial inhomogeneities in the incident laser beam. The phenomenon of light quenching has numerous potential applications in biophysics, such as studies of the orientation and dynamics of fluorescent macromolecules.Keywords
This publication has 15 references indexed in Scilit:
- Probing the transition stateNature, 1992
- Long-range correlations within DNANature, 1992
- Time-resolved fluorescence intensity and anisotropy decays of 2,5-diphenyloxazole by two-photon excitation and frequency-domain fluorometryThe Journal of Physical Chemistry, 1992
- Compliance of bacterial polyhooks measured with optical tweezersCytometry, 1991
- Two-Photon Laser Scanning Fluorescence MicroscopyScience, 1990
- Optical trapping and manipulation of single cells using infrared laser beamsNature, 1987
- A study of protein dynamics from anisotropy decays obtained by variable frequency phase-modulation fluorometry: internal motions of N-methylanthraniloyl melittinBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1986
- Rotational freedom of tryptophan residues in proteins and peptidesBiochemistry, 1983
- Dynamic properties of the lipid-water interface of model membranes as revealed by lifetime-resolved fluorescence emission spectraBiochemistry, 1981
- Fluorescence anisotropy measurements under oxygen quenching conditions as a method to quantify the depolarizing rotations of fluorophores. Application to diphenylhexatriene in isotropic solvents and in lipid bilayersBiochemistry, 1979