scholarly journals Thermodynamics and Mesomechanics of Nanostructural Transitions in Biological Membranes as Liquid Crystals

Author(s):  
Lev Panin
2001 ◽  
Vol 15 (09n10) ◽  
pp. 299-308
Author(s):  
MARIA HONCIUC ◽  
ELENA SLAVNICU

The latest studies in biophysics and biochemistry have revealed the major role that liquid crystals (LC) and related phenomena play in biological processes. To account for a number of membrane mechanisms in view of the theoretical model developed by S. J. Singer, studies were carried out on mixtures of fatty acids (arachidic, lauric, butyric) and cholesterol in different weight percentages. Such mixtures may help one understand some mechanisms on which the operation of biological membranes relies. To this end, the way these mixtures behave in an electric field was studied. Electric measurements were conducted from which the average time of electric relaxation (τ) and average electric permittivity (ε r ) were determined. Depending on cholesterol percentage, changes by more than one order of magnitude were found to occur in the electric relaxation time. The ratio between the various fatty acid components did not influence the average time τ in any significant manner. By contrast, the relative electric permittivity ε r was seen to decrease by at least one order of magnitude with raising the cholesterol percentage. The electric properties of such systems essentially depend on changing the amount of cholesterol in the system.


Author(s):  
S.W. Hui ◽  
D.F. Parsons

The development of the hydration stages for electron microscopes has opened up the application of electron diffraction in the study of biological membranes. Membrane specimen can now be observed without the artifacts introduced during drying, fixation and staining. The advantages of the electron diffraction technique, such as the abilities to observe small areas and thin specimens, to image and to screen impurities, to vary the camera length, and to reduce data collection time are fully utilized. Here we report our pioneering work in this area.


Author(s):  
Neng-Bo He ◽  
S.W. Hui

Monolayers and planar "black" lipid membranes have been widely used as models for studying the structure and properties of biological membranes. Because of the lack of a suitable method to prepare these membranes for electron microscopic observation, their ultrastructure is so far not well understood. A method of forming molecular bilayers over the holes of fine mesh grids was developed by Hui et al. to study hydrated and unsupported lipid bilayers by electron diffraction, and to image phase separated domains by diffraction contrast. We now adapted the method of Pattus et al. of spreading biological membranes vesicles on the air-water interfaces to reconstitute biological membranes into unsupported planar films for electron microscopic study. hemoglobin-free human erythrocyte membrane stroma was prepared by hemolysis. The membranes were spreaded at 20°C on balanced salt solution in a Langmuir trough until a surface pressure of 20 dyne/cm was reached. The surface film was repeatedly washed by passing to adjacent troughs over shallow partitions (fig. 1).


Author(s):  
M. Locke ◽  
J. T. McMahon

The fat body of insects has always been compared functionally to the liver of vertebrates. Both synthesize and store glycogen and lipid and are concerned with the formation of blood proteins. The comparison becomes even more apt with the discovery of microbodies and the localization of urate oxidase and catalase in insect fat body.The microbodies are oval to spherical bodies about 1μ across with a depression and dense core on one side. The core is made of coiled tubules together with dense material close to the depressed membrane. The tubules may appear loose or densely packed but always intertwined like liquid crystals, never straight as in solid crystals (Fig. 1). When fat body is reacted with diaminobenzidine free base and H2O2 at pH 9.0 to determine the distribution of catalase, electron microscopy shows the enzyme in the matrix of the microbodies (Fig. 2). The reaction is abolished by 3-amino-1, 2, 4-triazole, a competitive inhibitor of catalase. The fat body is the only tissue which consistantly reacts positively for urate oxidase. The reaction product is sharply localized in granules of about the same size and distribution as the microbodies. The reaction is inhibited by 2, 6, 8-trichloropurine, a competitive inhibitor of urate oxidase.


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