Paclitaxel suppresses Tau-mediated microtubule bundling in a concentration-dependent manner

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dc.contributor.authorChoi, Myung-Chulko
dc.contributor.authorChung, Peter Jko
dc.contributor.authorSong, Chaeyeonko
dc.contributor.authorMiller, Herbert Pko
dc.contributor.authorKiris, Eko
dc.contributor.authorLid, Youliko
dc.contributor.authorWilson, Leslieko
dc.contributor.authorFeinstein, Stuart Cko
dc.contributor.authorSafinya, Cyrus Rko
dc.date.accessioned2017-01-12T07:12:37Z-
dc.date.available2017-01-12T07:12:37Z-
dc.date.created2016-12-27-
dc.date.created2016-12-27-
dc.date.created2016-12-27-
dc.date.issued2017-01-
dc.identifier.citationBIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, v.1861, no.1, pp.3456 - 3463-
dc.identifier.issn0304-4165-
dc.identifier.urihttp://hdl.handle.net/10203/218286-
dc.description.abstractBackground: Microtubules (MTs) are protein nanotubes comprised of straight protofilaments (PFs), head to tail assemblies of alpha beta-tubulin heterodimers. Previously, it was shown that Tau, a microtubule-associated protein (MAP) localized to neuronal axons, regulates the average number of PFs in microtubules with increasing inner radius <R-in(MT)> observed for increasing Tau/tubulin-dimer molar ratio Phi(Tau) at paclitaxel/tubulin-dimer molar ratio Lambda(ptxl) = 1/1. Methods: We report a synchrotron SAXS and TEM study of the phase behavior of microtubules as a function of varying concentrations of paclitaxel (1/32 <= Lambda(ptxl) <= 1/4) and Tau (human isoform 3RS, 0 <= Phi(3Rs) <= 1/2) at room temperature. Results: Tau and paclitaxel have opposing regulatory effects on microtubule bundling architectures and microtubule diameter. Surprisingly and in contrast to previous results at Air = 1/1 where microtubule bundles are absent, in the lower paclitaxel concentration regime (Lambda(ptxl) <= 1/4), we observe both microtubule doublets and triplets with increasing Tau. Furthermore, increasing paditaxel concentration (up to Lambda(ptxl) = 1/1) slightly decreased the average microtubule diameter (by similar to 1 PF) while increasing Tau concentration (up to Phi(3RS) = 1/2) significantly increased the diameter (by similar to 2-3 PFs). Conclusions: The suppression of Tau-mediated microtubule bundling with increasing paclitaxel is consistent with paditaxel seeding more, but shorter, microtubules by rapidly exhausting tubulin available for polymerization. Microtubule bundles require the aggregate Tau-Tau attractions along the microtubule length to overcome individual microtubule thermal energies disrupting bundles. General significance: Investigating MAP-mediated interactions between microtubules (as it relates to in vivo behavior) requires the elimination or minimization of paclitaxel. (C) 2016 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectX-RAY-SCATTERING-
dc.subjectFORMATION IN-VITRO-
dc.subjectTHERMAL FLUCTUATIONS-
dc.subjectDYNAMIC INSTABILITY-
dc.subjectPROTEIN-TAU-
dc.subjectTUBULIN-
dc.subjectTAXOL-
dc.subjectPROTOFILAMENTS-
dc.subjectBINDING-
dc.subjectDOMAINS-
dc.titlePaclitaxel suppresses Tau-mediated microtubule bundling in a concentration-dependent manner-
dc.typeArticle-
dc.identifier.wosid000390736300050-
dc.identifier.scopusid2-s2.0-84994528965-
dc.type.rimsART-
dc.citation.volume1861-
dc.citation.issue1-
dc.citation.beginningpage3456-
dc.citation.endingpage3463-
dc.citation.publicationnameBIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS-
dc.identifier.doi10.1016/j.bbagen.2016.09.011-
dc.contributor.localauthorChoi, Myung-Chul-
dc.contributor.nonIdAuthorChung, Peter J-
dc.contributor.nonIdAuthorSong, Chaeyeon-
dc.contributor.nonIdAuthorMiller, Herbert P-
dc.contributor.nonIdAuthorKiris, E-
dc.contributor.nonIdAuthorLid, Youli-
dc.contributor.nonIdAuthorWilson, Leslie-
dc.contributor.nonIdAuthorFeinstein, Stuart C-
dc.contributor.nonIdAuthorSafinya, Cyrus R-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorTau-
dc.subject.keywordAuthorPaclitaxel-
dc.subject.keywordAuthorMicrotubule-
dc.subject.keywordAuthorSmall-angle X-ray scattering-
dc.subject.keywordPlusX-RAY-SCATTERING-
dc.subject.keywordPlusFORMATION IN-VITRO-
dc.subject.keywordPlusTHERMAL FLUCTUATIONS-
dc.subject.keywordPlusDYNAMIC INSTABILITY-
dc.subject.keywordPlusPROTEIN-TAU-
dc.subject.keywordPlusTUBULIN-
dc.subject.keywordPlusTAXOL-
dc.subject.keywordPlusPROTOFILAMENTS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusDOMAINS-
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