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pubmed-article:11983898pubmed:abstractTextWe developed a stochastic model of microtubule (MT) assembly dynamics that estimates tubulin-tubulin bond energies, mechanical energy stored in the lattice dimers, and the size of the tubulin-GTP cap at MT tips. First, a simple assembly/disassembly state model was used to screen possible combinations of lateral bond energy (DeltaG(Lat)) and longitudinal bond energy (DeltaG(Long)) plus the free energy of immobilizing a dimer in the MT lattice (DeltaG(S)) for rates of MT growth and shortening measured experimentally. This analysis predicts DeltaG(Lat) in the range of -3.2 to -5.7 k(B)T and DeltaG(Long) plus DeltaG(S) in the range of -6.8 to -9.4 k(B)T. Based on these estimates, the energy of conformational stress for a single tubulin-GDP dimer in the lattice is 2.1-2.5 k(B)T. Second, we studied how tubulin-GTP cap size fluctuates with different hydrolysis rules and show that a mechanism of directly coupling subunit addition to hydrolysis fails to support MT growth, whereas a finite hydrolysis rate allows growth. By adding rules to mimic the mechanical constraints present at the MT tip, the model generates tubulin-GTP caps similar in size to experimental estimates. Finally, by combining assembly/disassembly and cap dynamics, we generate MT dynamic instability with rates and transition frequencies similar to those measured experimentally. Our model serves as a platform to examine GTP-cap dynamics and allows predictions of how MT-associated proteins and other effectors alter the energetics of MT assembly.lld:pubmed
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pubmed-article:11983898pubmed:authorpubmed-author:CassimerisLyn...lld:pubmed
pubmed-article:11983898pubmed:authorpubmed-author:VanBurenVince...lld:pubmed
pubmed-article:11983898pubmed:authorpubmed-author:OddeDavid JDJlld:pubmed
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pubmed-article:11983898pubmed:pagination6035-40lld:pubmed
pubmed-article:11983898pubmed:dateRevised2010-9-14lld:pubmed
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pubmed-article:11983898pubmed:articleTitleEstimates of lateral and longitudinal bond energies within the microtubule lattice.lld:pubmed
pubmed-article:11983898pubmed:affiliationDepartment of Biological Sciences, Lehigh University, 111 Research Drive, Bethlehem, PA 18015, USA.lld:pubmed
pubmed-article:11983898pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11983898pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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