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Filipin Fluorescence Quenching by Spin-labeled Probes: Studies in Aqueous Solution and in a Membrane Model System

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1995 Jul 1
PMID 7669893
Citations 11
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Abstract

A detailed photophysical study of the fluorescence quenching (transient and steady state) of the macrolide antibiotic filipin by nitroxide-substituted fatty acids and a cholesterol derivative was carried out, aimed at determining its transverse position in a model system of membranes (multilamellar vesicles of dipalmitoylphosphatidylcholine). Filipin partitions efficiently into membranes (Kp = (5.0 +/- 1.0).10(3), 20 degrees C) and it was concluded that the antibiotic is buried in the membrane, away from the lipid-water interface. In addition, information on the organization of the quenchers was also obtained. The 5-nitroxide derivative of the fatty acid is essentially randomly distributed, while the 16-nitroxide is aggregated at concentrations higher than approximately 5% molar. For the cholesterol compound the results point to a phase separation at concentrations higher than 3% molar (below this limit concentration filipin associates with the derivatized sterol with KA = 20 M-1, assuming a 1:1 interaction). We propose that this phase separation and the aggregation state of filipin in the aqueous solution may be key processes in the antibiotic mode of action. A systematic and general approach to fluorescence quenching data analysis in complex (e.g., biochemical) systems is also presented.

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References
1.
Maurin L, Bancel F, Morin P, Bienvenue A . Interactions between a paramagnetic analogue of cholesterol and filipin. Biochim Biophys Acta. 1988; 939(1):102-10. DOI: 10.1016/0005-2736(88)90051-x. View

2.
Song P, Chae Q, Fujita M, Baba H . Electronic relaxation processes in retinol and retinal: anomalous external heavy-atom effects and temperature dependence of fluorescence. J Am Chem Soc. 1976; 98(3):819-24. DOI: 10.1021/ja00419a032. View

3.
Castanho M, Brown W, Prieto M . Filipin and its interaction with cholesterol in aqueous media studied using static and dynamic light scattering. Biopolymers. 1994; 34(4):447-56. DOI: 10.1002/bip.360340402. View

4.
Ruggiero A, Hudson B . Critical density fluctuations in lipid bilayers detected by fluorescence lifetime heterogeneity. Biophys J. 1989; 55(6):1111-24. PMC: 1330577. DOI: 10.1016/S0006-3495(89)82908-X. View

5.
Severs N, Robenek H . Detection of microdomains in biomembranes. An appraisal of recent developments in freeze-fracture cytochemistry. Biochim Biophys Acta. 1983; 737(3-4):373-408. DOI: 10.1016/0304-4157(83)90007-2. View