Cholesterol has a concentration-dependent effect on membrane organization. It is able to control the membrane permeability by inducing conformational ordering of the lipid chains. A systematic investigation of lipid bilayer permeability is described in the present work. It takes advantage of the transmembrane potential difference modulation induced in vesicles when an external electric field is applied. The magnitude of this modulation is under the control of the membrane electrical permeability. When brought to a critical value by the external field, the membrane potential difference induces a new membrane organization. The membrane is then permeable and prone to solubilized membrane protein back-insertion. This is obtained for an external field strength, which depends on membrane native permeability. This approach was used to study the cholesterol effect on phosphatidylcholine bilayers. Studies have been performed with lipids in gel and in fluid states. When cholesterol is present, it does not affect electropermeabilization and electroinsertion in lipids in the fluid state. When lipids are in the gel state, cholesterol has a dose-dependent effect. When present at 6% (mol/mol), cholesterol prevents electropermeabilization and electroinsertion. When cholesterol is present at more than 12%, electropermeabilization and electroinsertion are obtained under milder field conditions. This is tentatively explained by a cholesterol-induced alteration of the hydrophobic barrier of the bilayer core. Our results indicate that lipid membrane permeability is affected by the cholesterol content.
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http://dx.doi.org/10.1016/S0006-3495(99)77363-7 | DOI Listing |
Mol Membr Biol
May 2005
Institut de Pharmacologie et de Biologie Structurale du CNRS (UMR 5089), 205 route de Narbonne, F-31077 Toulouse cedex 4, France.
The C-terminal fragment of colicin, a protein that is highly soluble in aqueous solution, is spontaneously and irreversibly inserted into the membranes of mammalian cells, which are locally permeabilized by a transmembrane voltage increase. Insertion is detected by immunodetection. This is obtained by mixing the protein with electropermeabilized cells.
View Article and Find Full Text PDFBiophys J
April 1999
Institut de Pharmacologie et de Biologie Structurale du CNRS, UPR 9062, F-31062 Toulouse Cedex, France.
Cholesterol has a concentration-dependent effect on membrane organization. It is able to control the membrane permeability by inducing conformational ordering of the lipid chains. A systematic investigation of lipid bilayer permeability is described in the present work.
View Article and Find Full Text PDFEur J Biochem
December 1997
Institut de Pharmacologie et de Biologie Structurale du CNRS, Toulouse, France.
Back insertion of a solubilized membrane protein, glycophorin A, has been obtained in lipid multilamellar vesicles by applying calibrated electric field pulses on a lipid/protein mixture. Experimental evidence for insertion is given by means of immunofluorescence. Insertion was obtained only under field conditions that induced the leakage of a soluble hydrophilic molecule, calcein, which was trapped between the lipid layers.
View Article and Find Full Text PDFJ Biol Chem
October 1997
Institut de Pharmacologie et de Biologie Structurale du CNRS, 118 rte de Narbonne, F-31062 Toulouse Cedex, France.
Previously we demonstrated that transmembrane back insertion of glycophorin A, a solubilizable intrinsic protein, can be obtained in dipalmitoylphosphatidylcholine multilamellar vesicles, MLVs, by electropulsation (Raffy, S., and Teissié, J. (1995) Eur.
View Article and Find Full Text PDFEur J Biochem
June 1995
Dept III: Glycoconjugués et Biomembranes, CNRS, Toulouse, France.
Transmembraneous back-insertion of a solubilized membrane protein, glycophorin A, has been obtained in 1,2 dipalmitoyl-sn-glycero-3-phosphocholine (Pam2GroPCho) cell-size-like liposomes by submitting the lipid/protein mixture to calibrated electric field pulses. Field conditions which are prone to trigger glycophorin insertion are similar to those which mediate lipid layer electropermeabilization. The efflux of calcein, trapped in the liposomes during their preparation, was observed only when field strength is higher than 1.
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