Abstract

The phylum of Apicomplexa groups intracellular parasites that employ substrate-dependent gliding motility to invade host cells, egress from the infected cells and cross biological barriers. The glideosome associated connector (GAC) is a conserved protein essential to this process. GAC facilitates the association of actin filaments with surface transmembrane adhesins and the efficient transmission of the force generated by myosin translocation of actin to the cell surface substrate. Here, we present the crystal structure of Toxoplasma gondii GAC and reveal a unique, supercoiled armadillo repeat region that adopts a closed ring conformation. Characterisation of the solution properties together with membrane and F-actin binding interfaces suggest that GAC adopts several conformations from closed to open and extended. A multi-conformational model for assembly and regulation of GAC within the glideosome is proposed.

Data availability

Diffraction data have been deposited in PDB under the accession code 8C4A.The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD039335.All data generated or analysed during this study are included in the manuscript, figures and supplementary files.

The following data sets were generated

Article and author information

Author details

  1. Amit Kumar

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  2. Oscar Vadas

    Department of Microbiology and Molecular Medicine, University of Geneva, Geneva, Switzerland
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3511-6479
  3. Nicolas Dos Santos Pacheco

    Department of Microbiology and Molecular Medicine, University of Geneva, Geneva, Switzerland
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-1959-194X
  4. Xu Zhang

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  5. Kin Chao

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  6. Nicolas Darvill

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  7. Helena Ø Rasmussen

    Department of Chemistry, Aarhus University, Aarhus, Denmark
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-8384-656X
  8. Yingqi Xu

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  9. Gloria Meng-Hsuan Lin

    Department of Microbiology and Molecular Medicine, University of Geneva, Geneva, Switzerland
    Competing interests
    No competing interests declared.
  10. Fisentzos A Stylianou

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  11. Jan Skov Pedersen

    Department of Chemistry, Aarhus University, Aarhus, Denmark
    Competing interests
    No competing interests declared.
  12. Sarah L Rouse

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  13. Marc L Morgan

    Department of Life Sciences, Imperial College London, London, United Kingdom
    Competing interests
    No competing interests declared.
  14. Dominique Soldati-Favre

    Department of Microbiology and Molecular Medicine, University of Geneva, Geneva, Switzerland
    Competing interests
    Dominique Soldati-Favre, Senior editor, eLife.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4156-2109
  15. Stephen Matthews

    Department of Life Sciences, Imperial College London, London, United Kingdom
    For correspondence
    s.j.matthews@imperial.ac.uk
    Competing interests
    No competing interests declared.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-0676-0927

Funding

Leverhulme Trust (RPG_2018_107)

  • Stephen Matthews

Biotechnology and Biological Sciences Research Council (BB/W001764/1)

  • Stephen Matthews

Swiss Re Foundation (10030_185325)

  • Dominique Soldati-Favre

Swiss Re Foundation (CRSII5_198545)

  • Dominique Soldati-Favre

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

Copyright

© 2023, Kumar 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. Amit Kumar
  2. Oscar Vadas
  3. Nicolas Dos Santos Pacheco
  4. Xu Zhang
  5. Kin Chao
  6. Nicolas Darvill
  7. Helena Ø Rasmussen
  8. Yingqi Xu
  9. Gloria Meng-Hsuan Lin
  10. Fisentzos A Stylianou
  11. Jan Skov Pedersen
  12. Sarah L Rouse
  13. Marc L Morgan
  14. Dominique Soldati-Favre
  15. Stephen Matthews
(2023)
Structural and regulatory insights into the glideosome-associated connector from Toxoplasma gondii
eLife 12:e86049.
https://doi.org/10.7554/eLife.86049

Share this article

https://doi.org/10.7554/eLife.86049

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