Lipid assembled

The lipid molecule is the main constituent of biological cell membranes. In aqueous solutions amphiphilic lipid molecules form self-assembled structures such as bilayer vesicles, inverse hexagonal and multi-lamellar patterns, and so on. Among these lipid assemblies, construction of the lipid bilayer on a solid substrate has long attracted much attention due to the many possibilities it presents for scientific and practical applications [4]. Use of an artificial lipid bilayer often gives insight into important aspects ofbiological cell membranes [5-7]. The wealth of functionality of this artificial structure is the result of its own chemical and physical properties, for example, two-dimensional fluidity, bio-compatibility, elasticity, and rich chemical composition. 

We thank Dr. M. Hirano at Toray Research Center, Kamakura for providing us with the purified PS II. We also thank Dr. H. Minamikawa for the synthesis of Maln(Phyt)2 and Dr. K. Kawasaki for the FFEM experiments. This work was performed as a part of a R D project of AIST (subject Physical properties of membrane protein/lipid assemblies) and of International Joint Research Program FY 2001-2002 supported by NEDO. 

Lipid assemblies of the lamellar type, such as lipid bilayers, can feature a true phase transition in which the topology does not change. Upon cooling, the bilayer goes from the fluid phase to the gel phase. In the fluid phase, the acyl chains are disordered, in the sense that there is enough free volume around the chains to allow for chain conformation variations. In the gel phase, the acyl chains are more densely packed and believed to be ordered in an all-trans (straight) configuration. For very pure systems, at temperatures below this sharp gel-to-liquid phase transition, there are several other states and distinct transitions detectable (pre-transition, ripple phase, etc.). These phases will not be reviewed here. In biomembranes, many type of lipids (and other molecules) occur, and it is known that for this reason the gel-to-liquid phase transition is... 

This review emphasizes an intriguing and potentially useful aspect of the polymerization of lipid assemblies, i.e. polymerization and domain formation within an ensemble of molecules that is usually composed of more than one amphiphile. General aspects of domain formation in binary lipid mixtures and the polymerization of lipid bilayers are discussed in Sects. 1.1 and 1.2, respectively. More detailed reviews of these topics are available as noted. The mutual interactions of lipid domains and lipid polymerization are described in the subsequent sections. Given the proper circumstances the polymerization of lipid monolayers or bilayers can lock in the phase separation of lipids, i.e. pre-existing lipid domains within the ensemble as described in Sect. 2. Section 3 reviews the evidence for the polymerization-initiated phase separation of polymeric domains from the unpolymerized lipids. 

The structure of biological and model membranes is frequently viewed in the context of the fluid mosaic model [4], Since biological membranes are composed of a mixture of various lipids, proteins, and carbohydrates the supra-structure or lateral organization of the components is not necessarily random. In order to model biological membranes, lipid assemblies of increasing complexity were studied. Extensive investigation of multicomponent monolayers (at the air-water interface) as well as bilayers have been reported. 

Kleinschmidt JH, Tamm LK (2002) Structural transitions in short-chain lipid assemblies studied by P-31-NMR spectroscopy. Biophys J 83 994—1003... 

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