J. Lipid Res.
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Originally published In Press as doi:10.1194/jlr.M200136-JLR200 on October 16, 2002

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Journal of Lipid Research, Vol. 44, 65-71, January 2003
Copyright © 2003 by Lipid Research, Inc.

Biomimetic lipid/polymer colorimetric membranes

: molecular and cooperative properties

Sofiya Kolusheva*, Ellen Wachtel{dagger} and Raz Jelinek1,*

* Department of Chemistry and Stadler Minerva Center for Mesoscopic Macromolecular Engineering, Ben Gurion University of the Negev, Beersheva 84105, Israel
{dagger} Chemical Services Unit, Weizmann Institute of Science, Rehovot 76100, Israel

1 To whom correspondence should be addressed. e-mail: razj{at}bgumail.bgu.ac.il

Characterization of membranes and of biological processes occurring within membranes is essential for understanding fundamental cellular behavior. Here we present a detailed biophysical study of a recently developed colorimetric biomimetic membrane assembly constructed from physiological lipid molecules and conjugated polydiacetylene. Various analytical techniques have been applied to characterize the organization of the lipid components in the chromatic vesicles and their contributions to the observed blue-to-red color transitions. Experiments reveal that both the polymerized units as well as the lipids exhibit microscopic phases and form domains whose properties and bilayer organization are interdependent. These domains are interspersed within mixed lipid/polymer vesicles that have a size distribution different from those of aggregates of the individual molecular constituents.

The finding that fluidity changes induced within the lipid domains are correlated with the chromatic transitions demonstrates that the colorimetric platform can be used to evaluate the effects of individual molecular components, such as negatively charged lipids and cholesterol, upon membrane fluidity and thermal stability.

Abbreviations: DLS, dynamic light scattering; DMPC, dimyristoylphosphatidylcholine; DMPG, dimyristoylphosphatidylglycerol; DSC, differential scanning calorimetry; ESR, electron spin resonance; PDA, polydiacetylene; PE-(NBD), 1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine-N-(7-nitro-2-1,3-benzoxadiol-4-yl); SAXS, small angle X-ray scattering; uv, ultra-violet

Supplementary key words phospholipids • polydiacetylenes • small angle X-ray scattering • biosensors


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