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Membrane compartment theory

It is obvious why the spectroscopist wants to investigate the structure of integral membrane proteins or enzymes, whose biological action is linked to the presence of phospholipids such as phospholipase, in a membrane-mimicking environment Why such an environment should also be used for other peptides like hormones becomes more clear when we take into account the membrane compartment theory [10-12] as postulated by R. Schwyzer. This theory states that peptides that target membrane-embedded receptors... [Pg.95]

Fig. 4.—Compartment Theory of Starch Synthesis. (Key MM, membrane permeable to D-gluoose and maltosacoharides of DP 4 (1), D-enzyme (2) hexokinase-adenosine 5-triphosphate (3), phosphoglucomutase (4), P-enzyme with maltotetraose primer (5), Q-enzyme.)... Fig. 4.—Compartment Theory of Starch Synthesis. (Key MM, membrane permeable to D-gluoose and maltosacoharides of DP 4 (1), D-enzyme (2) hexokinase-adenosine 5-triphosphate (3), phosphoglucomutase (4), P-enzyme with maltotetraose primer (5), Q-enzyme.)...
The simplest practicable approach considers the membrane as a continuous, nonporous phase in which water of hydration is dissolved.In such a scenario, which is based on concentrated solution theory, the sole thermodynamic variable for specifying the local state of the membrane is the water activity the relevant mechanism of water back-transport is diffusion in an activity gradient. However, pure diffusion models provide an incomplete description of the membrane response to changing external operation conditions, as explained in Section 6.6.2. They cannot predict the net water flux across a saturated membrane that results from applying a difference in total gas pressures between cathodic and anodic gas compartments. [Pg.398]

The surface compartment model (SCM)14,15, which is a theory of ion transport focused on ionic process in electrical double layers at membrane protein surfaces, can explain these phenomena. The steady state physical properties of the discrete surface compartments are calculated from electrical double layer theory. [Pg.373]

Based on Donnan s [18, 19] and Onsager s [41, 42] fundamental works, the theories for Donnan dialysis systems were developed [20-26, 32-36]. The BAHLM system could be considered as two DD systems, operating in consecutive order, continuously in one module (see Fig. 6.2) the first is composed of feed/LM and the second is composed of LM/strip compartments, separated by ion-exchange membranes. Therefore, the Kedem-Katchalsky equations [43, 44] can be applied to our case ... [Pg.282]

Suppose a vessel is separated into two compartments by a semipermeable membrane which permits water and crystalloids, but not colloidal particles, to pass through. If water is placed in both the compartments and then some NaCl is added to one compartment, the NaCl will diffuse through the membrane and after a time become equally distributed in the water of both the compartments. However, if an ion which cannot pass through is placed on one side of the membrane, the distribution of a freely diffusible electrolyte like NaCl, becomes unequal in the solutions on the opposit sides of the membrane. This observation made in 1911 by Donnan is known after his name as Donnan s equalibrium theory. A theroretical derivation of this generalisation based on considerations of kinetics is given below. [Pg.380]

Positive measurements of second virial coefficients are considered due to attraction of solvent across a membrane to a second compartment containing the macromolecules considered (43, 44). The second virial coefficient is also a function of the cohesion between molecules, whereas, according to the theories of Van der Waals and Berthelot, the third virial coefficient is not. As hyaluronic acid tends to associate at low pH, the theoretical assumption of force additivity is denied. [Pg.236]

Surface/Diffusion Potential Theory. " The transmembrane potential, E, is expressed as a difference between the electrical potential, Ei, and Eo of the two bulk phases in the two aqueous compartments separated by a membrane or as a sum of phase boundary potentials produced at the membrane-electrolyte interfaces and the diffusion potential within the membrane arising from the movement of ionic species through the membrane (Figure 28). [Pg.75]

The electron transfer processes of photosynthesis and carbohydrate metabolism drive the flow of protons across the membranes of specialized cellular compartments. The chemiosmotic theory, discussed in Chapter 5, describes how the energy stored in a proton gradient across a membrane can be used to synthesize adenosine triphosphate (ATP), a mobile energy carrier. Intimate knowledge of thermodynamics and chemical kinetics is required to understand the details of the theory cuid the experiments that eventually verified it. [Pg.618]

The enzymatic activity of our lipid bodies preparations was unexpected. Lipid bodies membranes seem to be generated by the outer moiety of endoplasmic reticulum [12] our results are in line with that theory. On the other hand, the possibility exist that hydrophobic proteins from different cellular compartments might become bound to, or inserted into, lipid bodies membranes during subcellular fractionation, thus generating an artifact. Since we extensively washed our lipid bodies and the transferase activities are still present, we presume that the detected xylosyl transferases are tighly bound. [Pg.246]

Osmosis is a phenomenon of great importance in many applications and particularly so in polymer science. It is a very accurate and sensitive method of determining M and provides a useful application of the theories of solution thermodynamics developed in Section 3.1. The apparatus used for measuring osmotic pressure is shown schematically in Fig. 3.9. It consists essentially of a chamber with two compartments separated by a semi-permeable membrane. In one compartment there is pure solvent and in the other there is a polymer solution and both are at the same temperature. The membrane is permeable only to solvent molecules and is not permeable to polymer molecules. If both of the compartments are at the same pressure initially it is found that solvent molecules tend to diffuse from the pure solvent through the membrane and the diffusion stops only when the pressure in the solution compartment is increased by either applying an external pressure or allowing a pressure head to develop. The pressure which is required to stop solvent diffusion across the membrane is called the osmotic pressure. [Pg.106]


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See also in sourсe #XX -- [ Pg.95 ]




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