In situ architecture of the ER-mitochondria encounter structure

Nature. 2023 Jun;618(7963):188-192. doi: 10.1038/s41586-023-06050-3. Epub 2023 May 10.

Abstract

The endoplasmic reticulum and mitochondria are main hubs of eukaryotic membrane biogenesis that rely on lipid exchange via membrane contact sites1-3, but the underpinning mechanisms remain poorly understood. In yeast, tethering and lipid transfer between the two organelles is mediated by the endoplasmic reticulum-mitochondria encounter structure (ERMES), a four-subunit complex of unresolved stoichiometry and architecture4-6. Here we determined the molecular organization of ERMES within Saccharomyces cerevisiae cells using integrative structural biology by combining quantitative live imaging, cryo-correlative microscopy, subtomogram averaging and molecular modelling. We found that ERMES assembles into approximately 25 discrete bridge-like complexes distributed irregularly across a contact site. Each bridge consists of three synaptotagmin-like mitochondrial lipid binding protein domains oriented in a zig-zag arrangement. Our molecular model of ERMES reveals a pathway for lipids. These findings resolve the in situ supramolecular architecture of a major inter-organelle lipid transfer machinery and provide a basis for the mechanistic understanding of lipid fluxes in eukaryotic cells.

MeSH terms

  • Endoplasmic Reticulum* / chemistry
  • Endoplasmic Reticulum* / metabolism
  • Lipids
  • Mitochondria* / chemistry
  • Mitochondria* / metabolism
  • Mitochondrial Membranes / metabolism
  • Models, Molecular
  • Saccharomyces cerevisiae Proteins / chemistry
  • Saccharomyces cerevisiae Proteins / metabolism
  • Saccharomyces cerevisiae* / chemistry
  • Saccharomyces cerevisiae* / cytology
  • Saccharomyces cerevisiae* / metabolism
  • Synaptotagmins / chemistry
  • Synaptotagmins / metabolism

Substances

  • Lipids
  • Saccharomyces cerevisiae Proteins
  • Synaptotagmins