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Biophys J, December 2002, p. 3380-3392, Vol. 83, No. 6
*Biophysics Graduate Group, Division of Biological Sciences, and
Department of Chemical Engineering and Material Science,
University of California, Davis, Davis, California 95616 USA
Proteins and other macromolecules are believed to hinder
molecular lateral diffusion in cellular membranes. We have constructed a well-characterized model system to better understand how obstacles in
lipid bilayers obstruct diffusion. Fluorescence recovery after photobleaching was used to measure the lateral diffusion coefficient in
single supported bilayers composed of mixtures of
1,2-dilauroylphosphotidylcholine (DLPC) and
1,2-distearoylphosphotidylcholine (DSPC). Because these lipids are
immiscible and phase separate at room temperature, a novel quenching
technique allowed us to construct fluid DLPC bilayers containing small
disk-shaped gel-phase DSPC domains that acted as obstacles to lateral
diffusion. Our experimental setup enabled us to analyze the same
samples with atomic force microscopy and exactly characterize the size,
shape, and number of gel-phase domains before measuring the
obstacle-dependent diffusion coefficient. Lateral obstructed diffusion
was found to be dependent on obstacle area fraction, size, and
geometry. Analysis of our results using a free area diffusion model
shows the possibility of unexpected long-range ordering of fluid-phase
lipids around the gel-phase obstacles. This lipid ordering has
implications for lipid-mediated protein interactions in cellular membranes.
Biophys J, December 2002, p. 3380-3392, Vol. 83, No. 6
© 2002 by the Biophysical Society 0006-3495/02/12/3380/13 $2.00
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