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* Department of Chemistry and Chemical Biology, Indiana University-Purdue University, Indianapolis, Indiana;
Institut für Mikrosystemtechnik, Universität Freiburg, Freiburg, Germany; and
Lehrstuhl für Makromolekulare Stoffe, Department Chemie, Technische Universität München, Munich, Germany
Correspondence: Address reprint requests to Christoph A. Naumann, E-mail: naumann{at}chem.iupui.edu.
The degree of domain registration in a liquid-ordered/liquid-disordered phase-separating lipid mixture consisting of 1-stearoyl-2-oleoyl-sn-3-phosphocholine, egg sphingomyelin, and cholesterol (molar mixing ratio of 1:1:1) was studied using three different planar lipid bilayer architectures distinguished by their bilayer-substrate distance d using epifluorescence microscopy. The bilayer systems, which were built layer by layer using Langmuir-Blodgett/Schaefer film depositions, included a solid-supported bilayer (d
15 Å) and two polymer-supported bilayers with d
30 Å and d
58 Å, respectively. Complete domain registration between Langmuir-Blodgett and Schaefer monolayer domains was observed for d
58 Å but not in the cases when d
15 Å and d
30 Å. Building the bilayer layer by layer guaranteed that any preexisting domains were not in registration initially; our data show that the domain registration observed was not caused by lipid flip-flop or by lateral rearrangement of preexisting large-scale domains. Instead, additional studies on bilayer systems with asymmetric lipid composition indicate that preexisting domains in the Langmuir-Blodgett monolayer induce the formation of completely registered domains in the opposite Schaefer monolayer. This study provides insight into possible biophysical mechanisms of transbilayer domain coupling. Our findings support the concept that the formation of transbilayer signaling platforms based on registered raft domains may occur without the active involvement of membrane-spanning proteins.
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