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Characterization of Horizontal Lipid Bilayers as a Model System to Study Lipid Phase Separation

Authors :
Honigmann, Alf
Walter, Claudius
Erdmann, Frank
Eggeling, Christian
Wagner, Richard
Source :
Biophysical Journal; June 2010, Vol. 98 Issue: 12 p2886-2894, 9p
Publication Year :
2010

Abstract

Artificial lipid membranes are widely used as a model system to study single ion channel activity using electrophysiological techniques. In this study, we characterize the properties of the artificial bilayer system with respect to its dynamics of lipid phase separation using single-molecule fluorescence fluctuation and electrophysiological techniques. We determined the rotational motions of fluorescently labeled lipids on the nanosecond timescale using confocal time-resolved anisotropy to probe the microscopic viscosity of the membrane. Simultaneously, long-range mobility was investigated by the lateral diffusion of the lipids using fluorescence correlation spectroscopy. Depending on the solvent used for membrane preparation, lateral diffusion coefficients in the range Dlat= 10–25 μm2/s and rotational diffusion coefficients ranging from Drot= 2.8 − 1.4 × 107s−1were measured in pure liquid-disordered (Ld) membranes. In ternary mixtures containing saturated and unsaturated phospholipids and cholesterol, liquid-ordered (Lo) domains segregated from the Ldphase at 23°C. The lateral mobility of lipids in Lodomains was around eightfold lower compared to those in the Ldphase, whereas the rotational mobility decreased by a factor of 1.5. Burst-integrated steady-state anisotropy histograms, as well as anisotropy imaging, were used to visualize the rotational mobility of lipid probes in phase-separated bilayers. These experiments and fluorescence correlation spectroscopy measurements at different focal diameters indicated a heterogeneous microenvironment in the Lophase. Finally, we demonstrate the potential of the optoelectro setup to study the influence of lipid domains on the electrophysiological properties of ion channels. We found that the electrophysiological activity of gramicidin A (gA), a well-characterized ion-channel-forming peptide, was related to lipid-domain partitioning. During liquid-liquid phase separation, gA was largely excluded from Lodomains. Simultaneously, the number of electrically active gA dimers increased due to the increased surface density of gA in the Ldphase.

Details

Language :
English
ISSN :
00063495 and 15420086
Volume :
98
Issue :
12
Database :
Supplemental Index
Journal :
Biophysical Journal
Publication Type :
Periodical
Accession number :
ejs21631960
Full Text :
https://doi.org/10.1016/j.bpj.2010.03.033