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Photosensitizer Binding to Lipid Bilayers As a Precondition for the Photoinactivation of Membrane Channels

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2000 Apr 25
PMID 10777753
Citations 16
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Abstract

The photodynamic activity of sulfonated aluminum phthalocyanines (AlPcS(n), 1 </= n </= 4) was found to correlate with their affinity for membrane lipids. Adsorbing to the surface of large unilamellar vesicles (LUVs), aluminum phthalocyanine disulfonate induced the highest changes in their electrophoretic mobility. AlPcS(2) was also most efficient in mediating photoinactivation of gramicidin channels, as revealed by measurements of the electric current across planar lipid bilayers. The increase in the degree of sulfonation of phthalocyanine progressively reduced its affinity for the lipid bilayer as well as its potency of sensitizing gramicidin channel photoinactivation. The portion of photoinactivated gramicidin channels, alpha, increased with rising photosensitizer concentration up to some optimum. The concentration at which alpha was at half-maximum amounted to 80 nM, 30 nM, 200 nM, and 2 microM for AlPcS(1), AlPcS(2), AlPcS(3), and AlPcS(4), respectively. At high concentrations alpha was found to decrease, which was attributed to quenching of reactive oxygen species and self-quenching of the photosensitizer triplet state by its ground state. Fluoride anions were observed to inhibit both AlPcS(n) (2 </= n </= 4) binding to LUVs and sensitized photoinactivation of gramicidin channels. It is concluded that photosensitizer binding to membrane lipids is a prerequisite for the photodynamic inactivation of gramicidin channels.

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References
1.
Girotti A . Photodynamic lipid peroxidation in biological systems. Photochem Photobiol. 1990; 51(4):497-509. DOI: 10.1111/j.1751-1097.1990.tb01744.x. View

2.
Rokitskaya T, Antonenko Y, Kotova E . The interaction of phthalocyanine with planar lipid bilayers. Photodynamic inactivation of gramicidin channels. FEBS Lett. 1993; 329(3):332-5. DOI: 10.1016/0014-5793(93)80248-s. View

3.
Ben-Hur E, Malik Z, Dubbelman T, Margaron P, Ali H, van Lier J . Phthalocyanine-induced photohemolysis: structure-activity relationship and the effect of fluoride. Photochem Photobiol. 1993; 58(3):351-5. DOI: 10.1111/j.1751-1097.1993.tb09573.x. View

4.
Rosenthal I, Shafirovich V, Geacintov N, Ben-Hur E, Horowitz B . The photochemical properties of fluoroaluminum phthalocyanine. Photochem Photobiol. 1994; 60(3):215-20. DOI: 10.1111/j.1751-1097.1994.tb05093.x. View

5.
Kochevar I, Bouvier J, Lynch M, Lin C . Influence of dye and protein location on photosensitization of the plasma membrane. Biochim Biophys Acta. 1994; 1196(2):172-80. DOI: 10.1016/0005-2736(94)00236-3. View