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ULTIMATE COMPUTING - Quantum Consciousness Studies

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Cytoskeleton/Cytocomputer 99<br />

possess “ATPase activity,” that is they .contract conformationally due to<br />

hydrolysis of ATP. Dynein arms contract in waves and mediate sliding between<br />

the adjacent outer tubules to drive ciliary and flagellar motility. Dynein arms<br />

attached to MT in neuronal axons act collectively to pass material in “bucket<br />

brigade” axoplasmic transport. These and other MT “bending sidearms” will be<br />

discussed in Section 5.5.2.<br />

Other MAPs are bridges between parallel MT, filaments, organelles and the<br />

“microtrabecular lattice” and appear to integrate microtubules with the rest of the<br />

cytoplasm (Figure 5.6). MAPs from mammalian brain neurons have been<br />

characterized into three main groups. These are high molecular weight (greater<br />

than 100 kilodalton) MAP 1 and MAP 2, and a number of closely related 56–62<br />

kilodalton proteins designated as “tau.” <strong>Studies</strong> in rats show an increase in<br />

number and an altered distribution of the various forms of tubulin, high molecular<br />

weight MAPs, and tau which correlate with rat brain development and learning.<br />

Both MAP 2 and tau are heat stable, stimulate MT polymerization (lower Cc) and<br />

share binding domains on intact MT; they are heterogeneous protein families<br />

whose functions are unknown. MAP 2 is concentrated in cell bodies and dendrites<br />

of neurons, found in a ratio of MAP 2 to tubulin of one to twelve, occurs in only<br />

small amounts in axons and is absent in glia. Conversely, brain tau is largely<br />

confined to axons. Both MAP 2 and tau are phosphorylated by cyclic AMP<br />

dependent protein kinases, proteins which amplify effects of calcium ions.<br />

Intracellular levels of calcium ions, in turn, are regulated by diverse extracellular<br />

signals including neurotransmitters, hormones and electrical factors to regulate<br />

cell shape, motility, secretory processes and other functions. Thus these MAPs<br />

can mediate diverse inputs into the cytoskeleton. Each MAP attached to an MT<br />

may function like a “synapse” in a parallel, laterally interconnected network.

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