Structural basis of mitochondrial tethering by mitofusin complexes

Science. 2004 Aug 6;305(5685):858-62. doi: 10.1126/science.1099793.

Abstract

Vesicle fusion involves vesicle tethering, docking, and membrane merger. We show that mitofusin, an integral mitochondrial membrane protein, is required on adjacent mitochondria to mediate fusion, which indicates that mitofusin complexes act in trans (that is, between adjacent mitochondria). A heptad repeat region (HR2) mediates mitofusin oligomerization by assembling a dimeric, antiparallel coiled coil. The transmembrane segments are located at opposite ends of the 95 angstrom coiled coil and provide a mechanism for organelle tethering. Consistent with this proposal, truncated mitofusin, in an HR2-dependent manner, causes mitochondria to become apposed with a uniform gap. Our results suggest that HR2 functions as a mitochondrial tether before fusion.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Animals
  • Cell Line
  • Crystallography, X-Ray
  • Dimerization
  • GTP Phosphohydrolases / chemistry*
  • GTP Phosphohydrolases / metabolism*
  • Humans
  • Hybrid Cells
  • Hydrophobic and Hydrophilic Interactions
  • Intracellular Membranes / physiology
  • Intracellular Membranes / ultrastructure
  • Membrane Fusion
  • Mice
  • Mitochondria / metabolism*
  • Mitochondria / ultrastructure
  • Models, Molecular
  • Molecular Sequence Data
  • Mutation
  • Protein Structure, Secondary
  • Protein Structure, Tertiary

Substances

  • GTP Phosphohydrolases
  • Mfn1 protein, mouse
  • Mfn2 protein, mouse

Associated data

  • PDB/1T3J