Membranes, structural order

An important aspect of membrane structure is the orientation or ordering of lipid molecules in the bilayer. In the bilayers sketched in Figures 9.2 and 9.4, the long axes of the lipid molecules are portrayed as being perpendicular (or... 

FIG. 2 Example media (a) Surfactant-water phase diagram. (Reprinted from Ref. 206, Copyright 1991, with permission from Elsevier Science.) (b) Ordered periodic and bicontinuous structures. (Reprinted from Ref. 178 with permission from Academic Press, Ltd.) (c) Nonordered membrane structures from ternary microemulsions. (Reprinted with permission from Ref. 177, Copyright 1989, American Chemical Society.)... 

The basic reactions of thiolsulfonates have been known for sometime (Field et al., 1961, 1964), but more recently, they have been applied to the study of protein interactions by site-directed modification of native cysteines or through modification of cysteines introduced at particular points in proteins by mutagenesis. Such studies have yielded insights into the structure and binding site characteristics of proteins (Kirley, 1989). Pascual et al. (1998) used AEAETS to probe the acetylcholine receptor from the extracellular side of the membrane in order to investigate the molecular accessibility and electrostatic potential within the open and closed channel. 

All of the above considerations have sometimes led to a too rigid picture of the membrane structure. Of course, the mentioned types of fluctuations (protrusions, fluctuations in area per molecule, chain interdigitations) do exist and will turn out to be important. Without these, the membrane would lack any mechanism to, for example, adjust to the environmental conditions or to accommodate additives. Here we come to the central theme of this review. In order to come to predictive models for permeation in, and transport through bilayers, it is necessary to go beyond the surfactant parameter approach and the fluid mosaic model. 

The formalism sketched above has been used in the literature in more or less the same detail by many authors [87-92]. The predicted membrane structure that follows from this strategy has one essential problem the main gel-to-liquid phase transition known to occur in lipid membranes is not recovered. It is interesting to note that one of the first computer models of the bilayer membrane by Marcelja [93] did feature a first-order phase transition. This author included nematic-like interactions between the acyl tail, similar to that used in liquid crystals. This approach was abandoned for modelling membranes in later studies, because this transition was (unfortunately) lost when the molecules were described in more detail [87]. 

Biological membranes fluidity order parameters lipid-protein interactions translational diffusion site accessibility structural changes membrane potentials complexes and binding energy-linked and light-induced changes effects of additives location of proteins lateral organization and dynamics... 

F. Jahnig, Structural order of lipids and proteins in membranes Evaluation of fluorescence anisotropy data, Proc. Natl. Acad. Sci. U.SA. 76, 6361-6365 (1979). 

Proton exchange membranes (PEMs) are a key component in PEM fuel cells (PEMECs) and an area of active research in commercial, government, and academic institutions. In this chapter, the review of PEM materials is divided into two sections. The first will cover the most important properties of a membrane in order for it to perform adequately within a PEMFC. The latter part of this chapter will then provide an overview of existing PEM materials from both academic and industrial research facilities. Wherever possible, the membranes will also be discussed with respect to known structure-property relationships. 

In order to interpret the physicochemical steps of retinal transduction as well as membrane excitability, we analyze macroscopic properties of membranes within biological components. Such membranes separate two aqueous ionic phases the chemical compositions of which are kept constant separately. The total flux through the membrane is directly deduced from the counterbalance quantities in order to maintain the involved thermodynamical affinities constant. From such measurement, we calculate the dynamical membrane permeability. This permeability depends not only on membrane structure but also on internal chemical reactions. 

Although there are several sites of first contact between a foreign compound and a biological system, the absorption phase (and also distribution and excretion) necessarily involves the passage across cell membranes whichever site is involved. Therefore, it is important first to consider membrane structure and transport in order to understand the absorption of toxic compounds. 

In recent years, membrane bioreactors, bioreactors combined with membrane separation unit have established themselves as an alternative configuration for traditional bioreactors. The important advantages offered by membrane bioreactors are the several different types of membrane modules, membrane structures, materials commercially available. Membrane bioreactors seem particularly suited to carry out complex enzymatic/microbial reactions and/or to separate, in situ, the product in order to increase the reaction efficiency. The membrane bioreactor is a new generation of the biochemical/chemical reactors that offer a wide variety of applications for producing new chemical compounds, for treatment of wastewater, and so on. 

Fluorescence techniques have also been used to determine the localization of molecules in membranes. Using this technique, the localization of the linear dye molecule 3,3 -diethyloxadicarboxyamine iodide (DODCI) in lipid bilayer vesides was determined as a function of lipid chain length and unsaturation. It was found that the fraction of the dye in the interior region of the membrane was decreased as a function of chain length in the order C12 > C14 > C16 > C18. In unsaturated lipids it was Ci4 i > C14 0 > C16 1 > C16 0, which is in agreement with the general observation that the penetration of amphiphilic molecules into the interior of membranes increases with an increase in the fluidity of the membrane structure [59]. 

---