ULTIMATE COMPUTING - Quantum Consciousness Studies
ULTIMATE COMPUTING - Quantum Consciousness Studies
ULTIMATE COMPUTING - Quantum Consciousness Studies
- No tags were found...
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
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.