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In situ architecture of the ER-mitochondria encounter structure.
Wozny, Michael R; Di Luca, Andrea; Morado, Dustin R; Picco, Andrea; Khaddaj, Rasha; Campomanes, Pablo; Ivanovic, Lazar; Hoffmann, Patrick C; Miller, Elizabeth A; Vanni, Stefano; Kukulski, Wanda.
Afiliação
  • Wozny MR; MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Di Luca A; Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
  • Morado DR; Department of Biology, University of Fribourg, Fribourg, Switzerland.
  • Picco A; MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Khaddaj R; SciLifeLab, Solna, Sweden.
  • Campomanes P; Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Ivanovic L; Department of Biochemistry, University of Geneva, Geneva, Switzerland.
  • Hoffmann PC; Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland.
  • Miller EA; Department of Biology, University of Fribourg, Fribourg, Switzerland.
  • Vanni S; Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland.
  • Kukulski W; Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland.
Nature ; 618(7963): 188-192, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37165187
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Retículo Endoplasmático / Mitocôndrias Tipo de estudo: Prognostic_studies Idioma: En Revista: Nature Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Retículo Endoplasmático / Mitocôndrias Tipo de estudo: Prognostic_studies Idioma: En Revista: Nature Ano de publicação: 2023 Tipo de documento: Article