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ULTIMATE COMPUTING - Quantum Consciousness Studies

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Models of Cytoskeletal Computing 165<br />

MT which comprise the axopod are explained by inter MT bridges of two<br />

different lengths. The authors considered that these two types of linkages can not<br />

only account for the complex structure of the axopod, but also indicate two<br />

different conformational states of the tubulin dimers to which the bridges attach.<br />

Along the lengths of the axopod, microtubule linkages are found at intervals that<br />

reflect binding at approximately every fourth dimer. These precise linkage sites<br />

represented a code of some sort to Roth, Pihlaja, and Shigenaka who proposed in<br />

1970 that recurrent patterns, or “gradients” existed in microtubules to localize<br />

these precise binding patterns. They defined these patterns as “gradions”:<br />

repeating conformational sequences or fields in which multiple varying patterns<br />

can exist in the same molecular architecture simultaneously.<br />

Figure 8.3: “Gradions” within microtubule lattice. Dark shaded dimers are MAP<br />

attachment patterns; numbered dimers are determined by proximity to MAP<br />

attachment sites. MAP binding and other “gradionators” are thought to induce<br />

coded patterns representing information. From Roth, Pihlaja and Shigenaka<br />

(1970) by Paul Jablonka.<br />

Conformational states of individual tubulin subunits were thought to be<br />

controlled by factors Roth, Pihlaja, and Shigenaka termed “gradionators.” These<br />

could include ligand induced conformation, tubulin isozyme, detyrosination, or<br />

binding of MAPs including inter-microtubule bridges. They defined discrete

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