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Structural and mechanistic insights into the bacterial amyloid secretion channel CsgG

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  • Parveen Goyal

    (Structural and Molecular Microbiology, Structural Biology Research Center, VIB, Pleinlaan 2, 1050 Brussels, Belgium
    Structural Biology Brussels, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium)

  • Petya V. Krasteva

    (Unité G5 Biologie structurale de la sécrétion bactérienne, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France
    UMR 3528, CNRS, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France)

  • Nani Van Gerven

    (Structural and Molecular Microbiology, Structural Biology Research Center, VIB, Pleinlaan 2, 1050 Brussels, Belgium
    Structural Biology Brussels, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium)

  • Francesca Gubellini

    (Unité G5 Biologie structurale de la sécrétion bactérienne, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France
    UMR 3528, CNRS, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France)

  • Imke Van den Broeck

    (Structural and Molecular Microbiology, Structural Biology Research Center, VIB, Pleinlaan 2, 1050 Brussels, Belgium
    Structural Biology Brussels, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium)

  • Anastassia Troupiotis-Tsaïlaki

    (Structure et Fonction des Membranes Biologiques (SFMB), Université Libre de Bruxelles)

  • Wim Jonckheere

    (Structural and Molecular Microbiology, Structural Biology Research Center, VIB, Pleinlaan 2, 1050 Brussels, Belgium
    Structural Biology Brussels, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium)

  • Gérard Péhau-Arnaudet

    (UMR 3528, CNRS, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France)

  • Jerome S. Pinkner

    (Washington University in Saint Louis School of Medicine, St Louis, Missouri 63110-1010, USA)

  • Matthew R. Chapman

    (Cellular and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109-1048, USA)

  • Scott J. Hultgren

    (Washington University in Saint Louis School of Medicine, St Louis, Missouri 63110-1010, USA)

  • Stefan Howorka

    (Institute for Structural and Molecular Biology, University College London)

  • Rémi Fronzes

    (Unité G5 Biologie structurale de la sécrétion bactérienne, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France
    UMR 3528, CNRS, Institut Pasteur, 25–28 rue du Docteur Roux, 75015 Paris, France)

  • Han Remaut

    (Structural and Molecular Microbiology, Structural Biology Research Center, VIB, Pleinlaan 2, 1050 Brussels, Belgium
    Structural Biology Brussels, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium)

Abstract

CsgG and CgsE form an encaging translocon for selective, iterative diffusion of curli subunits across the non-energized bacterial outer membrane.

Suggested Citation

  • Parveen Goyal & Petya V. Krasteva & Nani Van Gerven & Francesca Gubellini & Imke Van den Broeck & Anastassia Troupiotis-Tsaïlaki & Wim Jonckheere & Gérard Péhau-Arnaudet & Jerome S. Pinkner & Matthew , 2014. "Structural and mechanistic insights into the bacterial amyloid secretion channel CsgG," Nature, Nature, vol. 516(7530), pages 250-253, December.
    • Handle: RePEc:nat:nature:v:516:y:2014:i:7530:d:10.1038_nature13768
    DOI: 10.1038/nature13768
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    Cited by:

    1. Hema M. Swasthi & Joseph L. Basalla & Claire E. Dudley & Anthony G. Vecchiarelli & Matthew R. Chapman, 2023. "Cell surface-localized CsgF condensate is a gatekeeper in bacterial curli subunit secretion," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

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