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Tau mediates microtubule bundle architectures mimicking fascicles of microtubules found in the axon initial segment

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  • Peter J. Chung

    (Molecular, Cellular, University of California)

  • Chaeyeon Song

    (Molecular, Cellular, University of California)

  • Joanna Deek

    (University of California
    Present address: Department of Physics, Technische Universität München, 85748 Garching, Germany.)

  • Herbert P. Miller

    (Neuroscience Research Institute and Molecular, Cellular, University of California)

  • Youli Li

    (Materials Research Laboratory, University of California)

  • Myung Chul Choi

    (Korea Advanced Institute of Science and Technology (KAIST))

  • Leslie Wilson

    (Neuroscience Research Institute and Molecular, Cellular, University of California)

  • Stuart C. Feinstein

    (Neuroscience Research Institute and Molecular, Cellular, University of California)

  • Cyrus R. Safinya

    (Molecular, Cellular, University of California)

Abstract

Tau, an intrinsically disordered protein confined to neuronal axons, binds to and regulates microtubule dynamics. Although there have been observations of string-like microtubule fascicles in the axon initial segment (AIS) and hexagonal bundles in neurite-like processes in non-neuronal cells overexpressing Tau, cell-free reconstitutions have not replicated either geometry. Here we map out the energy landscape of Tau-mediated, GTP-dependent ‘active’ microtubule bundles at 37 °C, as revealed by synchrotron SAXS and TEM. Widely spaced bundles (wall-to-wall distance Dw–w≈25–41 nm) with hexagonal and string-like symmetry are observed, the latter mimicking bundles found in the AIS. A second energy minimum (Dw–w≈16–23 nm) is revealed under osmotic pressure. The wide spacing results from a balance between repulsive forces, due to Tau’s projection domain (PD), and a stabilizing sum of transient sub-kBT cationic/anionic charge–charge attractions mediated by weakly penetrating opposing PDs. This landscape would be significantly affected by charge-altering modifications of Tau associated with neurodegeneration.

Suggested Citation

  • Peter J. Chung & Chaeyeon Song & Joanna Deek & Herbert P. Miller & Youli Li & Myung Chul Choi & Leslie Wilson & Stuart C. Feinstein & Cyrus R. Safinya, 2016. "Tau mediates microtubule bundle architectures mimicking fascicles of microtubules found in the axon initial segment," Nature Communications, Nature, vol. 7(1), pages 1-9, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12278
    DOI: 10.1038/ncomms12278
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    Cited by:

    1. Phillip A. Kohl & Chaeyeon Song & Bretton J. Fletcher & Rebecca L. Best & Christine Tchounwou & Ximena Garcia Arceo & Peter J. Chung & Herbert P. Miller & Leslie Wilson & Myung Chul Choi & Youli Li & , 2024. "Complexes of tubulin oligomers and tau form a viscoelastic intervening network cross-bridging microtubules into bundles," Nature Communications, Nature, vol. 15(1), pages 1-15, December.

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