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Resolving bundled microtubules using anti-tubulin nanobodies

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  • Marina Mikhaylova

    (Faculty of Science, Utrecht University, Padualaan 8
    RG Neuroplasticity, Leibniz Institute for Neurobiology, Brenneckestr. 6
    Present address: University Medical Center Hamburg-Eppendorf, UKE, Center for Molecular Neurobiology, ZMNH, Falkenried 94, 20251 Hamburg, Germany)

  • Bas M. C. Cloin

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Kieran Finan

    (King’s College London, Guy’s Campus)

  • Robert van den Berg

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Jalmar Teeuw

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Marta M. Kijanka

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Mikolaj Sokolowski

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Eugene A. Katrukha

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Manuel Maidorn

    (University of Göttingen, Humboldtallee 23)

  • Felipe Opazo

    (University of Göttingen, Humboldtallee 23)

  • Sandrine Moutel

    (Institut Curie, Research Center, 26, rue d'Ulm
    CNRS UMR144, 26, rue d'Ulm
    Institut Curie, 26, rue d'Ulm)

  • Marylin Vantard

    (Inserm, U836, F-38000, Grenoble, France. Univ. Grenoble Alpes, Grenoble Institut des Neurosciences)

  • Frank Perez

    (Institut Curie, Research Center, 26, rue d'Ulm
    CNRS UMR144, 26, rue d'Ulm)

  • Paul M. P. van Bergen en Henegouwen

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Casper C. Hoogenraad

    (Faculty of Science, Utrecht University, Padualaan 8)

  • Helge Ewers

    (King’s College London, Guy’s Campus
    Present address: Freie Universität Berlin, Institut für Chemie und Biochemie, Thielalle 63, 14195 Berlin, Germany)

  • Lukas C Kapitein

    (Faculty of Science, Utrecht University, Padualaan 8)

Abstract

Microtubules are hollow biopolymers of 25-nm diameter and are key constituents of the cytoskeleton. In neurons, microtubules are organized differently between axons and dendrites, but their precise organization in different compartments is not completely understood. Super-resolution microscopy techniques can detect specific structures at an increased resolution, but the narrow spacing between neuronal microtubules poses challenges because most existing labelling strategies increase the effective microtubule diameter by 20–40 nm and will thereby blend neighbouring microtubules into one structure. Here we develop single-chain antibody fragments (nanobodies) against tubulin to achieve super-resolution imaging of microtubules with a decreased apparent diameter. To test the resolving power of these novel probes, we generate microtubule bundles with a known spacing of 50–70 nm and successfully resolve individual microtubules. Individual bundled microtubules can also be resolved in different mammalian cells, including hippocampal neurons, allowing novel insights into fundamental mechanisms of microtubule organization in cell- and neurobiology.

Suggested Citation

  • Marina Mikhaylova & Bas M. C. Cloin & Kieran Finan & Robert van den Berg & Jalmar Teeuw & Marta M. Kijanka & Mikolaj Sokolowski & Eugene A. Katrukha & Manuel Maidorn & Felipe Opazo & Sandrine Moutel &, 2015. "Resolving bundled microtubules using anti-tubulin nanobodies," Nature Communications, Nature, vol. 6(1), pages 1-7, November.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms8933
    DOI: 10.1038/ncomms8933
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    Cited by:

    1. Torben Johann Hausrat & Philipp C. Janiesch & Petra Breiden & David Lutz & Sabine Hoffmeister-Ullerich & Irm Hermans-Borgmeyer & Antonio Virgilio Failla & Matthias Kneussel, 2022. "Disruption of tubulin-alpha4a polyglutamylation prevents aggregation of hyper-phosphorylated tau and microglia activation in mice," Nature Communications, Nature, vol. 13(1), pages 1-18, December.

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