Nanoscale stiffness topography reveals structure and mechanics of the transport barrier in intact nuclear pore complexes (original) (raw)
- Letter
- Published: 24 November 2014
- Armin Kramer1,3 na1,
- Aksana A. Labokha4 nAff7,
- Dino Osmanović1,2,
- Ivan Liashkovich3,
- Elena V. Orlova5,
- Ian J. Ford1,2,
- Guillaume Charras1,6,
- Ariberto Fassati4 &
- …
- Bart W. Hoogenboom1,2
Nature Nanotechnology volume 10, pages 60–64 (2015)Cite this article
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Abstract
The nuclear pore complex (NPC) is the gate for transport between the cell nucleus and the cytoplasm. Small molecules cross the NPC by passive diffusion, but molecules larger than ∼5 nm must bind to nuclear transport receptors to overcome a selective barrier within the NPC1. Although the structure and shape of the cytoplasmic ring of the NPC are relatively well characterized2,3,4,5, the selective barrier is situated deep within the central channel of the NPC and depends critically on unstructured nuclear pore proteins5,6, and is therefore not well understood. Here, we show that stiffness topography7 with sharp atomic force microscopy tips can generate nanoscale cross-sections of the NPC. The cross-sections reveal two distinct structures, a cytoplasmic ring and a central plug structure, which are consistent with the three-dimensional NPC structure derived from electron microscopy2,3,4,5. The central plug persists after reactivation of the transport cycle and resultant cargo release, indicating that the plug is an intrinsic part of the NPC barrier. Added nuclear transport receptors accumulate on the intact transport barrier and lead to a homogenization of the barrier stiffness. The observed nanomechanical properties in the NPC indicate the presence of a cohesive barrier to transport and are quantitatively consistent with the presence of a central condensate of nuclear pore proteins in the NPC channel.
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Acknowledgements
The authors thank H. Oberleithner for the use of laboratory facilities, P. Vergani for assistance with the preparation of X. laevis oocytes, D. Görlich for the expression plasmids for importin β and Ran-mix, S. Frey for Rch1-IBB-MBP-GFP protein, R.P. Richter for providing the data presented in Supplementary Fig. 8, J. Grech for the electron microscopy image in Fig. 1a, M. Goldberg for the protocol for removal of the nuclear basket from the NPCs, J. Bailey and A.H. Harker for support in initializing the modelling work, R. Thorogate for assistance with the confocal microscopy measurements, C. Leung for assistance in formatting the figures and T. Duke (deceased) and G. Aeppli for proofreading the manuscript. This work was partially funded by the European Molecular Biology Organization (ALTF 757-2008 to A.K.), the Kazakh Ministry of Education and Science (A.B.), the Sackler Foundation (D.O.), the UK Biotechnology and Biological Sciences Research Council (BB/G011729/1 to B.W.H.) and the Wellcome Trust (083810/Z/07/Z to A.F.). G.C. is a Royal Society University Research Fellow.
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Author notes
- Aksana A. Labokha
Present address: Present address: MedImmune, Granta Park, Cambridge CB21 6GH, UK, - Aizhan Bestembayeva and Armin Kramer: These authors contributed equally to this work
Authors and Affiliations
- London Centre for Nanotechnology, University College London, 17–19 Gordon Street, London, WC1H 0AH, UK
Aizhan Bestembayeva, Armin Kramer, Dino Osmanović, Ian J. Ford, Guillaume Charras & Bart W. Hoogenboom - Department of Physics and Astronomy, University College, London, Gower Street, London, WC1E 6BT, UK
Aizhan Bestembayeva, Dino Osmanović, Ian J. Ford & Bart W. Hoogenboom - Institute of Physiology II, University of Münster, Robert-Koch Strasse 27b, 48149 Münster, Germany
Armin Kramer & Ivan Liashkovich - Division of Infection & Immunity, Wohl Virion Centre, MRC Centre for Medical Molecular Virology, University College London, Gower Street, London, WC1E 6BT, UK
Aksana A. Labokha & Ariberto Fassati - Department of Biological Sciences, Birkbeck College, Institute of Structural and Molecular Biology, Malet Street, London, WC1E 7HX, UK
Elena V. Orlova - Department of Cell and Developmental Biology, University College London, Gower Street, London, WC1E 6BT, UK
Guillaume Charras
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Contributions
A.B., A.K., A.L., I.L., G.C., A.F. and B.W.H. designed the experiments. A.B., A.K., A.L. and I.L. performed the experiments. A.B., A.K. and B.W.H., with support from E.V.O., performed the data analysis. D.O., I.J.F. and B.W.H. designed and performed the polymer modelling. A.F. and B.W.H. wrote the manuscript. All authors read and commented on the manuscript.
Corresponding authors
Correspondence toAriberto Fassati or Bart W. Hoogenboom.
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Bestembayeva, A., Kramer, A., Labokha, A. et al. Nanoscale stiffness topography reveals structure and mechanics of the transport barrier in intact nuclear pore complexes.Nature Nanotech 10, 60–64 (2015). https://doi.org/10.1038/nnano.2014.262
- Received: 29 November 2013
- Accepted: 13 October 2014
- Published: 24 November 2014
- Issue Date: January 2015
- DOI: https://doi.org/10.1038/nnano.2014.262