IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v5y2014i1d10.1038_ncomms4912.html
   My bibliography  Save this article

The full-length cell–cell fusogen EFF-1 is monomeric and upright on the membrane

Author

Listed:
  • Tzviya Zeev-Ben-Mordehai

    (Oxford Particle Imaging Centre, Wellcome Trust Centre for Human Genetics, University of Oxford)

  • Daven Vasishtan

    (Oxford Particle Imaging Centre, Wellcome Trust Centre for Human Genetics, University of Oxford)

  • C. Alistair Siebert

    (Oxford Particle Imaging Centre, Wellcome Trust Centre for Human Genetics, University of Oxford)

  • Kay Grünewald

    (Oxford Particle Imaging Centre, Wellcome Trust Centre for Human Genetics, University of Oxford)

Abstract

Fusogens are membrane proteins that remodel lipid bilayers to facilitate membrane merging. Although several fusogen ectodomain structures have been solved, structural information on full-length, natively membrane-anchored fusogens is scarce. Here we present the electron cryo microscopy three-dimensional reconstruction of the Caenorhabditis elegans epithelial fusion failure 1 (EFF-1) protein natively anchored in cell-derived membrane vesicles. This reveals a membrane protruding, asymmetric, elongated monomer. Flexible fitting of a protomer of the EFF-1 crystal structure, which is homologous to viral class-II fusion proteins, shows that EFF-1 has a hairpin monomeric conformation before fusion. These structural insights, when combined with our observations of membrane-merging intermediates between vesicles, enable us to propose a model for EFF-1 mediated fusion. This process, involving identical proteins on both membranes to be fused, follows a mechanism that shares features of SNARE-mediated fusion while using the structural building blocks of the unilaterally acting class-II viral fusion proteins.

Suggested Citation

  • Tzviya Zeev-Ben-Mordehai & Daven Vasishtan & C. Alistair Siebert & Kay Grünewald, 2014. "The full-length cell–cell fusogen EFF-1 is monomeric and upright on the membrane," Nature Communications, Nature, vol. 5(1), pages 1-9, September.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4912
    DOI: 10.1038/ncomms4912
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms4912
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms4912?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Su-Hyuk Ko & Kyung-Ah Cho & Xin Li & Qitao Ran & Zhijie Liu & Lizhen Chen, 2025. "GPX modulation promotes regenerative axonal fusion and functional recovery after injury through PSR-1 condensation," Nature Communications, Nature, vol. 16(1), pages 1-20, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4912. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.