Bilayer dispersion

Another example comes from the work of Johnson, et a/.18 These workers studied spin labels dissolved in lipid bilayer dispersions of dipalmitoylphos-phatidylcholine and cholesterol (9 1 by weight) in the hope that anisotropic rotational diffusion of the spin label would mimic the motion of the bilayer components. In addition to 5-DS, which is sensitive to rotational motion about the NO bond, they used the steroidal nitroxide 8, which tends to rotate about an axis perpendicular to the N-O bond. ESR measurements were carried out at both 9 and 35 GHz and at temperatures ranging from 30 to 30 °C. Rather different results were obtained with the two spin labels, largely as a result of the different axes of rotation. Because the rotation rates were very slow, ESR spectra appeared as powder patterns rather than isotropic spectra and special methods were needed to extract the motional data. 

Kunitake, T. Aqueous Bilayer Dispersions, Cast Multilayer Films and Langmuir-Blo%ett Films of Azobenzene Containing Amphiphile. Coll. Surf. 19, 225 (1986). 

Case of flat interfaces solubilization of a solute in bilayers dispersed in... 

Fig. 2.3. Differential scanning calorimeter trace of dipalmitoyl phosphatidylcholine bilayers dispersed in water. The reference pan contained distilled water.

Larger intrinsic membrane proteins may span the membrane with several helices and perform functional tasks that can be quantified by biochemical assays. Two different approaches have been employed to study the lipid-protein interaction. One is to purify and delipidate fransmembrane proteins and to reconstitute them with selectively deuter-ated lipids the other is to incorporate deuterated fatty acids or other deuterated substrates into biological membranes by means of the biosynthetic pathway. In the latter case, the intact biological membrane is compared with aqueous bilayer dispersions formed from the extracted lipids. In the following we will discuss examples for the two types of assays. 

In an extensive SFA study of protein receptor-ligand interactions, Leckband and co-workers [114] showed the importance of electrostatic, dispersion, steric, and hydrophobic forces in mediating the strong streptavidin-biotin interaction. Israelachvili and co-workers [66, 115] have measured the Hamaker constant for the dispersion interaction between phospholipid bilayers and find A = 7.5 1.5 X 10 erg in water. 

Phospholipids e.g. form spontaneously multilamellar concentric bilayer vesicles73 > if they are suspended e.g. by a mixer in an excess of aqueous solution. In the multilamellar vesicles lipid bilayers are separated by layers of the aqueous medium 74-78) which are involved in stabilizing the liposomes. By sonification they are dispersed to unilamellar liposomes with an outer diameter of 250-300 A and an internal one of 150-200 A. Therefore the aqueous phase within the liposome is separated by a bimolecular lipid layer with a thickness of 50 A. Liposomes are used as models for biological membranes and as drug carriers. 

The development of monoalkyl phosphate as a low skin irritating anionic surfactant is accented in a review with 30 references on monoalkyl phosphate salts, including surface-active properties, cutaneous effects, and applications to paste and liquid-type skin cleansers, and also phosphorylation reactions from the viewpoint of industrial production [26]. Amine salts of acrylate ester polymers, which are physiologically acceptable and useful as surfactants, are prepared by transesterification of alkyl acrylate polymers with 4-morpholinethanol or the alkanolamines and fatty alcohols or alkoxylated alkylphenols, and neutralizing with carboxylic or phosphoric acid. The polymer salt was used as an emulsifying agent for oils and waxes [70]. Preparation of pharmaceutical liposomes with surfactants derived from phosphoric acid is described in [279]. Lipid bilayer vesicles comprise an anionic or zwitterionic surfactant which when dispersed in H20 at a temperature above the phase transition temperature is in a micellar phase and a second lipid which is a single-chain fatty acid, fatty acid ester, or fatty alcohol which is in an emulsion phase, and cholesterol or a derivative. 

Thus, the column should completely resolve about 14 equally spaced peaks. It is seen from figure 1 that a peak capacity of 14 is not realized although most of the components are separated. This means that the column may not have been packed particularly well and/or the flow rate used was significantly above the optimum velocity that would provide the maximum efficiency. The mobile phase that was used was tetrahydrofuran which was sufficiently polar to deactivate the silica gel with a layer (or perhaps bilayer) of adsorbed solvent molecules yet was sufficiently dispersive to provide adequate sample... 

The presence of impurities like free fatty acids in egg or soybean phosphatidylcholine, or in the (semi)synthetic phosphatidylcholines (e.g., DMPC, DPPC, DSPC) can be detected by monitoring the electrophoretic behavior of liposome dispersions of these phospholipids in aqueous media with low ionic strength a negative charge will be found on these liposomes when free fatty acids are present in the bilayers. 

P 68] No detailed experimental protocol was given [61, 62,142,143]. Two reactant streams, the solution of the reactant in hexane and concentrated sulfuric acid, were fed separately in a specially designed micro reactor by pumping action. There, a bilayer was formed initially, potentially decomposed to a dispersion, and led to rapid mass transfer between the phases. From this point, temperature was controlled by counter-flow heat exchange between the reaction channel and surrounding heat-transfer channel. The reaction was typically carried out at temperatures from 0 to 50 °C and using residence times of only a few seconds. If needed, a delay loop of... 

The artificial lipid bilayer is often prepared via the vesicle-fusion method [8]. In the vesicle fusion process, immersing a solid substrate in a vesicle dispersion solution induces adsorption and rupture of the vesicles on the substrate, which yields a planar and continuous lipid bilayer structure (Figure 13.1) [9]. The Langmuir-Blodgett transfer process is also a useful method [10]. These artificial lipid bilayers can support various biomolecules [11-16]. However, we have to take care because some transmembrane proteins incorporated in these artificial lipid bilayers interact directly with the substrate surface due to a lack of sufficient space between the bilayer and the substrate. This alters the native properties of the proteins and prohibits free diffusion in the lipid bilayer [17[. To avoid this undesirable situation, polymer-supported bilayers [7, 18, 19] or tethered bilayers [20, 21] are used. 

Recent studies [193] of the CO oxidation activity exhibited by highly dispersed nano-gold (Au) catalysts have reached the following conclusions (a) bilayer structures of Au are critical (b) a strong interaction between Au and the support leads to wetting and electron rich Au (c) oxidative environments deactivate Au catalyst by re-ox-idizing the support, which causes the Au to de-wet and sinter. Recent results have shown that the direct intervention of the support is not necessary to facilitate the CO oxidation reaction therefore, an Au-only mechanism is sufficient to explain the reaction kinetics. 

Liposomes are formed due to the amphiphilic character of lipids which assemble into bilayers by the force of hydrophobic interaction. Similar assemblies of lipids form microspheres when neutral lipids, such as triglycerides, are dispersed with phospholipids. Liposomes are conventionally classified into three groups by their morphology, i.e., multilamellar vesicle (MLV), small unilamellar vesicle (SUV), and large unilamellar vesicle (LUV). This classification of liposomes is useful when liposomes are used as models for biomembranes. However, when liposomes are used as capsules for drugs, size and homogeneity of the liposomes are more important than the number of lamellars in a liposome. Therefore, "sized" liposomes are preferred. These are prepared by extrusion through a polycarbonate... 

When these lipids are dispersed in water, they spontaneously form bilayer membranes (also called lamellae) which are composed of two monolayer sheets of lipid molecules with their hydrophobic surfaces facing one another and their hydrophilic surfaces contacting the aqueous medium. In the case of phospholipids such as phosphatidylcholine (10.50), the structure consists of ... 

Perhaps the simplest solvent dispersion method is that developed by Batzri and Korn (1973). Phospholipids and other lipids to be a part of the liposomal membrane are first dissolved in ethanol. This ethanolic solution then is rapidly injected into an aqueous solution of 0.16M KC1 using a syringe, resulting in a maximum concentration of no more than 7.5 percent ethanol. Using this method, single bilayer liposomes of about 25 nm diameter can be created that are... 

Other surface-active compounds self-assemble into bilayer structures (schematically illustrated in Fig. 10b), which normally spherilize into structures termed vesicles. When vesicles are formed from phospholipids, the term liposome is used to identify the structures, which also provide useful drug delivery systems [71]. Solutes may be dispersed into the lipid bilayer or into the aqueous interior, to be subsequently delivered through a variety of mechanisms. Liposomes have shown particular promise in their ability to act as modifiers for sustained or controlled release. 

The multilamellar bilayer structures that form spontaneously on adding water to solid- or liquid-phase phospholipids can be dispersed to form vesicular structures called liposomes. These are often employed in studies of bilayer properties and may be combined with membrane proteins to reconstitute functional membrane systems. A valuable technique for studying the properties of proteins inserted into bilayers employs a single bilayer lamella, also termed a black lipid membrane, formed across a small aperture in a thin partition between two aqueous compartments. Because pristine lipid bilayers have very low ion conductivities, the modifications of ion-conducting... 

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