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Published 30 July 2002. doi:10.1085/jgp.20028566
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© Rockefeller University Press, 0022-1295/2002/8/147/ $5.00
Journal of General Physiology, Volume 120, Number 2, August 2002 147-157

Interaction of A2E with Model Membranes. Implications to the Pathogenesis of Age-related Macular Degeneration

Soma De and Thomas P. Sakmar

Howard Hughes Medical Institute, Laboratory of Molecular Biology and Biochemistry, The Rockefeller University, New York, NY 10021

Address correspondence to Thomas P. Sakmar, Box 284, Rockefeller University, 1230 York Ave., New York, NY 10021. Fax (212) 327-7904; E-mail: sakmar{at}mail.rockefeller.edu

Deposition of a fluorophoric material, known as lipofuscin, in retinal pigment epithelium cells has been speculated to be one of the biomarkers of age-related macular degeneration. One of the fluorophores of lipofuscin has been characterized as A2E, a pyridinium bisretinoid. Its cationic nature along with two hydrophobic retinal chains suggests that it can disrupt the membrane integrity by its detergent-like activity and can thus cause cellular damage. With this notion, we studied in detail the interaction between A2E and the model membranes of different lipid compositions using fluorescence steady-state and fluorescence anisotropy measurements. A transition from vesicular to micellar structure occurred upon incorporation of A2E into the lipid bilayer. However, the A2E concentration at which this transition occurred depends on the lipid composition. A lipid mixture containing 10% phosphatidylserine (PS) (close to disc membrane PS content) behaved similarly to a lipid mixture having no PS. In contrast, vesicles containing 20% PS showed significantly different behavior. Membrane solubilization by A2E was also confirmed by vesicle leakage experiments. A2E also showed significant activity in liposome-mediated gene transfection. A lipid formulation containing 40% A2E and a helper lipid showed plasmid DNA transfection efficiency comparable to commercially available transfection reagents with no evidence of cytotoxicity. These results contribute to understanding the mechanism underlying the A2E-induced cellular dysfunction.

Key Words: lipofuscin • cellular dysfunction • lipid vesicles • fluorescence studies • membrane solubilization


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