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ULTIMATE COMPUTING - Quantum Consciousness Studies

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Cytoskeleton/Cytocomputer 89<br />

Figure 5.7: Microtubule mitotic spindles (wispy filaments separating<br />

chromosomes (heavy rods) establishing daughter cell polarity during cell division.<br />

Centrioles and MTOC are at nidus of each array. With permission from Marc<br />

DeBrabander (1982).<br />

MT vary markedly in stability and function. Structurally similar MT may be<br />

highly stable, or fleetingly transient. This variability can result from differences in<br />

tubulin chemistry, from effects of secondary proteins attached at specific points<br />

on MT surface lattices (microtubule associated proteins: MAPs), local<br />

cytoplasmic influences, membrane interactions and many other factors. Highly<br />

stable MT are found in cilia and flagella in which they are assembled into<br />

complex patterns and carry out their functions without disassembly. The other<br />

extreme are MT within mitotic spindles which separate chromosomes and<br />

establish daughter cell shape in cell division (“mitosis”—Figure 5.7). These<br />

“labile” MT not only assemble before mitosis and disassemble afterwards, but<br />

apparently undergo localized disassembly/reassembly during mitosis (“dynamic<br />

instability”). In some animal cells and during plant cell mitosis, assembly of MT<br />

subunits into MT appears to take place in the cytoplasm without any relation to a<br />

particular organelle. In other cells, structures including centrioles, basal bodies,<br />

centrosomes, and kinetochores facilitate assembly of microtubules at a specific<br />

site and orientation. These structures are called microtubule organizing centers<br />

(MTOC), and they consist of a pair of centrioles and a dense granular material. In<br />

general, negatively charged ends of MT attach to the MTOC, and positively<br />

charged ends grow distal to the MTOC, establishing cell polarity, shape and<br />

orientation.<br />

The MT assembly process may be tracked by parameters that crudely reflect<br />

the polymer level such as turbidity or viscosity. Generally, there is first a lag<br />

phase when no microtubules form, then a phase of exponential growth and finally<br />

a stable plateau. At low concentrations, no microtubules are formed. Above a

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