Lipid bilayer systems have been used extensively to study the structure and function of biomembranes including molecular recognition, permeation, adhesion, and fusion. 1-5 Further interest arises from their potential use as biosensors.6 , 7 While classical black lipid bilayer membranes are highly suitable as such model systems, they suffer from their limited long-term stability. 1 Additionally, to apply the broad range of surface sensitive experimental techniques developed in recent years for the characterization of ultrathin films, it is often necessary to immobilize lipid bilayers on solid supports. However, lateral fluidity of the lipid membrane is governed by the physical and chemical properties of the solid substrate. Thus, bilayer membranes prepared by the Langmuir-Blodgett (LB) technique or by vesicle fusion directly onto solid substrates are often polycrystalline or amorphous, and lateral lipid mobility within the membrane is restricted. While on hydrophilic oxidized silicon or glass a water layer (~1 nm thick) is formed which allows for free diffusion of phospholipid molecules (but not membrane-spanning proteins) within the bilayer,8 -10 on most other metals and metal oxides, lipid mobility is strongly suppressed.11 , 12 To preserve the membrane's natural properties, one promising approach is to rest it on a water-swellable (hydrophilic) polymer or polyelectrolyte cushion which can act as a deformable and mobile substrate6 , 13 , 14 like the cytoskeletal support in living cells. Such softly supported lipid bilayers can, in principle, exist in an entirely fluid state, nearly undisturbed by the presence of the supporting polymer gel which provides an aqueous compartment between the solid substrate and the membrane. In our recent work, we have studied DMPC bilayers on a highly branched cationic polymer (polyethylenimine, PEI). Important structural information about these polymer-supported bilayer systems formed by various preparation methods was provided by neutron scattering experiments.15 , 16 Furthermore, measuring the intermembrane interaction forces using the surface forces apparatus (SFA) technique has shown the effect of fluidity on membrane functionality.17These physisorbed, polymer-supported bilayers are only the first step in the approach of creating artificial biomembranes that more closely resemble living cells. To provide more biologically relevant architectures, molecular assemblies of increased complexity and longterm stability have been tested, including a partial chemical fixation of the membrane's lipids to the underlying polymeric substrate. 7,14,18,19 However, the construction of such "asymmetric" tethered supported membranes is not always straightforward, and each particular
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Author ManuscriptLangmuir. Author manuscript; available in PMC 2010 October 13.
NIH-PA Author ManuscriptNIH-PA Author Manuscript NIH-PA Author Manuscript system needs to be optimized. The most versatile approach appears to be vesicle fusion onto polymer-supported lipid monolayers previously prep...