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specific channel, the nicotinic acetylcholine receptor. This channel has been investigated in detail, because, among other reasons, it can be isolated in considerable quantities as the membranes of the cells forming the electric organ of electric fish are filled with this species. Acetylcholine, which is set free from vesicles present in the neighbourhood of the presynaptic membrane, is transferred into the recipient cell through this channel (Fig. 6.25). Once transferred it stimulates generation of a spike at the membrane of the recipient cell. The action of acetylcholine is inhibited by the enzyme, acetylcholinesterase, which splits acetylcholine to choline and acetic acid. Locomotion in higher organisms and other mechanical actions are made possible by the striated skeletal muscles. The basic structural unit of muscles is the muscle cell muscle fibre which is enclosed by a sarcoplasmatic membrane. This membrane invaginates into the interior of the fibre through transversal tubules which are filled with the intercellular liquid. The inside of the fibre consists of the actual sarcoplasm with inserted mitochondria, sarcoplasmatic reticulum and minute fibres called myofibrils, which are the organs of muscle contraction and relaxation. The membrane of the sarcoplasmatic reticulum contains Ca2+-ATPase, maintaining a concentration of calcium ions in the sarcoplasm of the relaxed muscle below 10~7mol dm~3. Under these conditions, the proteins, actin and myosin, forming the myofibrils lie in relative positions such that the muscle is relaxed. When a spike is transferred from the nerve fibre to the sarcoplasmatic membrane, another spike is also formed there which continues

A significant portion of the benefit that blades and virtualization bring is in the area of ease of implementation, deployment, and provisioning. This benefit can be measured by what is called time to return (on investment) or time to revenue. The modularity and prewiring of blade systems described previously work together to dramatically reduce the time needed initially to deploy blade

has even been suggested as a possible optical neural network element (Sumaru et al, 1999) Binding and transport properties can also be photoswitched (Weh et al, 1998; Anzai and Osa, 1994) In some systems the redox potential and ionic conductivity can be switched with light (Willner and Willner, 1997) Crown ethers (Zawisza et al, 1999; Tokuhisa et al, 1994) and calixarenes (Reynier et al, 1998) functionalized with azobenzene can be used as reversible ion-binding systems Thus, ion transport can be photoregulated In other cases, the transport properties can be photocontrolled not via binding but on the basis of changes in pore sizes (Sata et al, 2000; Abraham and Purushothaman, 1998; Kano et al, 1980) In a particularly elegant example, the size of nanochannels could be modi ed by irradiating azo ligands that decorate the channel walls (Liu et al, 2004).

Fig. 6.25 The nicotinic acetylcholine receptor in a membrane. The deciphering of the structure is based on X-ray diffraction and electron microscopy. (According to Kistler and coworkers) through the transverse tubules to the membrane of the sarcoplasmatic reticulum, increasing the permeability of the membrane for calcium ions by five orders within 1 millisecond, so that the concentration of Ca2+ ions in the sarcoplasm increases above 10~3 mol dm~3. This produces a relative shift of actin and myosin molecules and contraction of the muscle fibre. After disappearance of the spike, Ca2+-ATPase renews the original situation and the muscle is relaxed. 6.5.2 Membrane principles of bioenergetics The basic process by which living organisms obtain energy is photosynthesis in green plants, yielding carbonaceous substances (fuels) and oxidative phosphorylation in all organisms, in which the Gibbs energy obtained by oxidation of these carbonaceous substances with oxygen is converted into the energy of the polyphosphate bond in adenosinetriphosphate (ATP) through the reaction of adenosine diphosphate with dihydrogen phosphate ions (PinOrg)This process occurs in the mitochondria, organelles present in the cells of all multicellular organisms (see Figs 6.8 and 6.26). Mitochondria have two membranes. The invaginations of the internal membrane into the inner space of the organelle (matrix space) are termed crests (from the Latin, cristae). The oxidation of the carbonaceous substrate with oxygen cannot occur directly as the released energy would be converted into heat, but must proceed almost reversibly, through a number of poorly water-soluble redox

systems forming an electron transfer chain located in the internal membrane of the mitochondrion. They include the system of the oxidized and reduced forms of nicotinamide adenine dinucleotide (NAD + /NADH), several flavoprotein systems, especially FMN (flavinmononucleotide), Fe-S proteins (where the iron ions are bound in a complex with inorganic sulphide, cystein and a protein), coenzyme Q (ubiquinone) and several cytochromes. These redox systems are bound to phospholipids and other molecules in several integrated systems depending on their redox potential (see Table 6.2). The redox potentials of these systems, measured in solution, can be quite different from the potentials in the mitochondrial membrane. The sequence of the redox components in this electron transfer permits the oxidation of the carbonaceous substrates to occur 'vectorially', i.e. the chemical change is oriented in space. The theory of the accumulation of the Gibbs energy of oxidation of carbonaceous substrates in the form of the bond of the phosphate ion to