Transformation of taxol-stabilized microtubules into inverted tubulin tubules triggered by a tubulin conformation switch
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Bundles of taxol-stabilized microtubules (MTs) - hollow tubules comprised of assembled αβ-tubulin heterodimers - spontaneously assemble above a critical concentration of tetravalent spermine and are stable over long times at room temperature. Here we report that at concentrations of spermine several-fold higher the MT bundles (B MT) quickly become unstable and undergo a shape transformation to bundles of inverted tubulin tubules (B ITT), the outside surface of which corresponds to the inner surface of the B MT tubules. Using transmission electron microscopy and synchrotron small-angle X-ray scattering, we quantitatively determined both the nature of the B MT -to-B ITT transformation pathway, which results from a spermine-triggered conformation switch from straight to curved in the constituent taxol-stabilized tubulin oligomers, and the structure of the B ITT phase, which is formed of tubules of helical tubulin oligomers. Inverted tubulin tubules provide a platform for studies requiring exposure and availability of the inside, luminal surface of MTs to MT-targeted drugs and MT-associated proteins. © 2014 Macmillan Publishers Limited. All rights reserved.
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funding provided via
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2009271 Grant
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Consejo Nacional de Ciencia y Tecnología, CONACYT Grant
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DE-FG02-06ER46314 Grant
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Israel Science Foundation, ISF: 1372/13 Grant
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KAIST: HRHRP N10110077 Grant
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Ministry of Education, Science and Technology, MEST: R33-2008-000-10163-0 Grant
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National Institute of General Medical Sciences, NIGMS: R01GM059288 Grant
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National Institute of Neurological Disorders and Stroke, NINDS: R01NS013560 Grant
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National Institutes of Health, NIH Grant
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National Research Foundation of Korea, NRF: 2011-0030923, 2012R1A1A1011023, NRF 2011-0031931, NRF 2011-355-C00037 Grant
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National Science Foundation, NSF: 1101900, DMR-1101900 Grant
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Research
keywords
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Critical concentration; Heterodimers; Inner surfaces; Microtubules; Room temperature; Shape transformation; Synchrotron small-angle x-ray scatterings; Transformation pathways; Transmission electron microscopy; Oligomers; paclitaxel; tubulin; animal; article; binding site; cattle; chemistry; microtubule; protein binding; ultrastructure; Animals; Binding Sites; Cattle; Microtubules; Paclitaxel; Protein Binding; Tubulin
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