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ULTIMATE COMPUTING - Quantum Consciousness Studies

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Cytoskeleton/Cytocomputer 117<br />

through a series of serpentine maneuvers. Allen and colleagues concluded that the<br />

forces observed in their slithering free MT as well as in axoplasmic transport and<br />

ciliary bending are due to “force generating enzymes” directly attached to MT.<br />

Dynein, which functions to cause binding in cilia and flagella, is one MT force<br />

generating enzyme and kinesin is another motor for organelle transport along<br />

microtubules. Latex beads coated with kinesin translocate along microtubules<br />

similar to organelles, although at a slower velocity. Purifled kinesin can increase<br />

the frequency of axoplasmic organelle movement along purified MT.<br />

Allen and colleagues proposed the “backstroke hypothesis” which states that<br />

the force generating enzyme (dynein or kinesin) makes an elliptical stroke which<br />

imparts some force in both directions. Allen’s dynein backstroke model is capable<br />

of carrying vesicles in opposite directions simultaneously through sufficiently<br />

separated pathways so that they seldom collide. Further, the motion generated can<br />

be continuous, not interrupted by cycles of attachment and detachment. The<br />

mechanical cycle of each sidearm includes a radial stroke that moves vesicles in<br />

the anterograde direction toward the microtubule plus end. This part of the cycle<br />

also causes isolated MT to glide “retrograde.” The return stroke is tangential to<br />

the MT surface and transports the larger organelles in a retrograde pathway, and<br />

propels gliding MT toward their . “anterograde” plus end.<br />

The mechanisms by which the force generating protein arms may use ATP<br />

energy to contract will be discussed in Chapter 6. Even less well understood is the<br />

signaling and communication which orchestrates contractile activities of rows of<br />

arms spatially arrayed on MT lattices. Collective communication among MT<br />

lattice subunits (solitons, coherent excitations, lattice vibrations) could explain<br />

this orchestration.<br />

The backstroke model is currently favored more than another model:<br />

microstreams. Shimizu and Haken (1983) had proposed a dynamic cooperativity<br />

of cytoskeletal elements which generated hydrodynamic microstreams conveying<br />

cellular materials. They specifically focused on actin-myosin interactions to<br />

generate these microstreams. New techniques such as Nanovideo Microscopy<br />

developed by Marc DeBrabander and colleagues (1986) at Janssen Pharmaceutica<br />

Research Laboratories in Belgium show direct tracking of immunolabeled<br />

particles along MT, questioning the significance of microstreams. Particles are<br />

seen to travel in opposite directions along the same MT, passing each other like<br />

two railroad trains on adjacent tracks. Microstreaming does not appear dominant<br />

in axoplasmic transport, but could be important in other phenomena. The primary<br />

site of coordinated transport and its complex orchestration appears to rest solely<br />

in the province of MT.

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