Quenching of perylene fluorescence by Co2+ ions in dipalmitoylphosphatidylcholine (DPPC) vesicles

Journal of Fluorescence - Tập 3 - Trang 77-84 - 1993
A. S. Holmes1, D. J. S. Birch1, T. Salthammer2,3
1Department of Physics and Applied Physics, University of Strathclyde, Glasgow, Scotland, UK
2Institut für Physikalische und Theoretische Chemie der Technischen Universität Braunschweig, Braunschweig, Germany
3WKI-Fraunhofer-Arbeitsgruppe für Holzforschung, Braunschweig, Germany

Tóm tắt

We report the fluorescence quenching of perylene by CoCl2·6H2O in small unilamellar DPPC vesicles via energy transfer. At the probe-to-lipid ratio of 1∶200 and quencher to lipid ratios of ≥12.5∶1, donor-donor energy transfer between clustered perylene molecules was observed as well as energy transfer from the perylene molecules to cobalt ions bothabove andbelow the main phase transition temperature of the lipid. The fluorescence quenching of perylene by CoCl2·6H2O in the lipid gel state is shown to be well described by Förster long-range energy transfer when both donor-donor and donor-acceptor energy transfer are considered. In the liquid crystalline phase diffusion of the molecules is described as well as energy transfer. The interaction radiusR 0 for energy transfer from perylene to Co2+ is found to be ∼13.4±1.1 Å in the gel phase at 303 K, in good agreement with the theoretical value forR 0 of 13.9 Å. In the liquid crystalline phase at 323 K the lower value obtained forR 0, ∼11.3±1.6 Å, is attributed to saturation of the Co2+ ions at the interfacial region of the bilayer. A diffusion coefficient of (1.06±0.15)×10−6 cm2 s−1 is obtained for perylene-cobalt diffusion in the liquid crystalline phase at 323K.

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