Modeling Hsp70/Hsp40 interaction by multi-scale molecular simulations and co-evolutionary sequence analysis

  1. Duccio Malinverni
  2. Alfredo Jost Lopez
  3. Paolo De Los Rios
  4. Gerhard Hummer
  5. Alessandro Barducci  Is a corresponding author
  1. Faculté de Sciences de Base, École Polytechnique Fédérale de Lausanne - EPFL, Switzerland
  2. Max Planck Institute of Biophysics, Germany
  3. Inserm, U1054, France

Abstract

The interaction between the Heat Shock Proteins 70 and 40 is at the core of the ATPase regulation of the chaperone machinery that maintains protein homeostasis. However, the structural details of the interaction are still elusive and contrasting models have been proposed for the transient Hsp70/Hsp40 complexes. Here we combine molecular simulations based on both coarse-grained and atomistic models with co-evolutionary sequence analysis to shed light on this problem by focusing on the bacterial DnaK/DnaJ system. The integration of these complementary approaches resulted in a novel structural model that rationalizes previous experimental observations. We identify an evolutionarily conserved interaction surface formed by helix II of the DnaJ J-domain and a structurally contiguous region of DnaK, involving lobe IIA of the nucleotide binding domain, the inter-domain linker and the β-basket of the substrate binding domain.

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Author details

  1. Duccio Malinverni

    Laboratoire de Biophysique Statistique, Faculté de Sciences de Base, École Polytechnique Fédérale de Lausanne - EPFL, Lausanne, Switzerland
    Competing interests
    The authors declare that no competing interests exist.
  2. Alfredo Jost Lopez

    Max Planck Institute of Biophysics, Frankfurt am Main, Germany
    Competing interests
    The authors declare that no competing interests exist.
  3. Paolo De Los Rios

    Laboratoire de Biophysique Statistique, Faculté de Sciences de Base, École Polytechnique Fédérale de Lausanne - EPFL, Lausanne, Switzerland
    Competing interests
    The authors declare that no competing interests exist.
  4. Gerhard Hummer

    Max Planck Institute of Biophysics, Frankfurt am Main, Germany
    Competing interests
    The authors declare that no competing interests exist.
  5. Alessandro Barducci

    Inserm, U1054, Montpellier, France
    For correspondence
    alessandro.barducci@cbs.cnrs.fr
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-1911-8039

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (2012_149278 & 20020_163042/1)

  • Duccio Malinverni
  • Paolo De Los Rios

Max-Planck-Gesellschaft

  • Alfredo Jost Lopez
  • Gerhard Hummer

Agence Nationale de la Recherche (ANR-14-ACHN-0016)

  • Alessandro Barducci

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Copyright

© 2017, Malinverni et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

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  1. Duccio Malinverni
  2. Alfredo Jost Lopez
  3. Paolo De Los Rios
  4. Gerhard Hummer
  5. Alessandro Barducci
(2017)
Modeling Hsp70/Hsp40 interaction by multi-scale molecular simulations and co-evolutionary sequence analysis
eLife 6:e23471.
https://doi.org/10.7554/eLife.23471

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https://doi.org/10.7554/eLife.23471