Transformation of taxol-stabilized microtubules into inverted tubulin tubules triggered by a tubulin conformation switch

被引:58
作者
Ojeda-Lopez, Miguel A. [1 ]
Needleman, Daniel J. [1 ]
Song, Chaeyeon [2 ]
Ginsburg, Avi [3 ]
Kohl, Phillip A. [4 ]
Li, Youli [4 ]
Miller, Herbert P. [5 ,6 ]
Wilson, Leslie [5 ,6 ]
Raviv, Uri [3 ]
Choi, Myung Chul [2 ]
Safinya, Cyrus R. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Mat, Dept Phys, Mol Cellular & Dev Biol Dept, Santa Barbara, CA 93106 USA
[2] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
[3] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
[4] Univ Calif Santa Barbara, Mat Res Lab, Santa Barbara, CA 93106 USA
[5] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[6] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
基金
新加坡国家研究基金会; 以色列科学基金会; 美国国家科学基金会;
关键词
SYNCHROTRON X-RAY; DYNAMICS; FORM; TAU; DNA; PROTOFILAMENTS; CONDENSATION; FLEXIBILITY; NANOTUBES; LIPOSOMES;
D O I
10.1038/nmat3858
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Bundles of taxol-stabilized microtubules (MTs)-hollow tubules comprised of assembled alpha beta-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.
引用
收藏
页码:195 / 203
页数:9
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