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ULTIMATE COMPUTING - Quantum Consciousness Studies

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Cytoskeleton/Cytocomputer 111<br />

Figure 5.21: “Soluble” intracellular enzymes (circles) governed by the<br />

microtrabecular lattice (MTL: solid dark) and bordering region of ordered and<br />

vicinal water (within thin line). The dark circle is part of a cross sectional view.<br />

Clegg (1981) has proposed that dynamic activity within the MTL can regulate the<br />

enzymatic activity. By Paul Jablonka.<br />

Is the MTL/cytomatrix the final microfrontier of biological organization<br />

Current imaging techniques would not reveal smaller levels of organization, just<br />

as it took advances in electron microscopy to discover first the MT cytoskeleton<br />

and then later the MTL. Perhaps smaller, more intricate networks ranging down to<br />

the level of single peptide filaments might be present. With layers of ordered<br />

water and charged ions, such a solid state “infoplasm” could occupy nearly the<br />

entire volume of biological material.<br />

5.5 Cytoskeletal Motility<br />

Albrecht-Buehler (1985):<br />

Cell movement ... appears to be determined by some kind of<br />

chemical computer, the nature of which is beyond our present<br />

understanding.<br />

Cell motility was discovered by van Leeuwenhoek who observed flagella<br />

propelled sperm cells swimming in the 17th century. A variety of cytoplasmic<br />

movements include “amoeboid” creeping over a surface, internal streaming,<br />

axoplasmic transport, muscle contraction, ciliary and flagellar bending, and cell<br />

shape changes. These maneuverings are all engineered by a relatively small group<br />

of proteins whose net collective effects can be quite spectacular. For example,

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