Self-assembled films bilayer lipid membranes

Description of the different mimetic systems will be the starting point of the presentation (Sect. 2). Preparation and characterization of monolayers (Langmuir films), Langmuir-Blodgett (LB) films, self-assembled (SA) mono-layers and multilayers, aqueous micelles, reversed micelles, microemulsions, surfactant vesicles, polymerized vesicles, polymeric vesicles, tubules, rods and related SA structures, bilayer lipid membranes (BLMs), cast multibilayers, polymers, polymeric membranes, and other systems will be delineated in sufficient detail to enable the neophyte to utilize these systems. Ample references will be provided to primary and secondary sources. 

For decades, colloid and surface scientists have known that amphiphilic molecules such as phospholipids can self-assemble or self-organize themselves into supramolecular structures of bilayer lipid membranes (planar BLMs and spherical liposomes), emulsions, and micelles [2-4]. As a matter of fact, our current understanding of the structure and function of biomembranes can be traced to the studies of these experimental systems such as soap films and Langmuir monolayers, which have evolved as a direct consequence of applications of classical principles of colloid and interfacial chemistry. As already mentioned in Section I, the seminal work on the self-assembly of planar lipid bilayers and bilayer or black lipid membranes was carried out in 1959-1963. The idea started while one of the authors was reading a paperback edition of Soap Bubbles by C. 

Self-assembled monolayers have recently attracted much attention as a new methodology for molecular assembly [249, 342]. They enable highly organized chemical binding of molecules of interest to the surfaces of, e.g., metals, semiconductors, and insulators. The well-ordered structure of self-assembled monolayers is in sharp contrast with conventional Langmuir-Blodgett films and lipid bilayer membranes in terms of stability, uniformity, and manipulation. Functional molecules can be arranged unidirectionally at the molecular level on substrates when substituents which will self-assemble on the substrates are attached to a terminal of the molecules. The wide variety of examples reported to date include porphyrins and metalloporphyrins in self-assembled monolayers [299-339]. 

Lipid bilayer membranes tethered to plasma-polymerized films as hydrophilic supports were another concept introduced recently [28], The plasma polymerization of maleic anhydride (MAH-PP), e.g., has led to the synthesis of thin polymeric coatings that appear to be suitable to act as a reservoir for an aqueous phase and a cushion for lipid bilayers [29], A crucial requirement for the use of such polymers as water containing supports for lipid bilayer membranes is their adhesion to the substrate. In a previous study [30] covalent binding of MAH-PP films to gold supports was achieved by a self assembled alkylthiol adhesion layer. The previous work has shown that maleic anhydride, when polymerized at a low duty cycle, can behave as a polyelectrolyte. The thin polymer layers were found to have a very low electrical resistance (ca. lOOQcm2) after immersion and subsequent hydrolysis/swelling in aqueous buffer. 

The LB film prepared in the dark shows temperature dependent UV-vis absorption spectra. At lower temperatures, there is an electronic interaction between the fullerene moieties in the LB film. Upon heating over 47 C, which is the subphase transition temperature of the cast films of the fullerene lipid [28, 36], the electronic interaction of the fullerene moieties is loosened. The electronic interaction between the fullerene moieties can be controlled by the phase change of the film. The fundamental property of the self-assembled bilayer membrane film is maintained in the LB film prepared in the dark, indicating that the molecular orientations of the... 

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