Multivalent Rab interactions determine tether-mediated membrane fusion

Mol Biol Cell. 2017 Jan 15;28(2):322-332. doi: 10.1091/mbc.E16-11-0764. Epub 2016 Nov 16.

Abstract

Membrane fusion at endomembranes requires cross-talk between Rab GTPases and tethers to drive SNARE-mediated lipid bilayer mixing. Several tethers have multiple Rab-binding sites with largely untested function. Here we dissected the lysosomal HOPS complex as a tethering complex with just two binding sites for the Rab7-like Ypt7 protein to determine their relevance for fusion. Using tethering and fusion assays combined with HOPS mutants, we show that HOPS-dependent fusion requires both Rab-binding sites, with Vps39 being the stronger Ypt7 interactor than Vps41. The intrinsic amphipathic lipid packaging sensor (ALPS) motif within HOPS Vps41, a target of the vacuolar kinase Yck3, is dispensable for tethering and fusion but can affect tethering if phosphorylated. In combination, our data demonstrate that a multivalent tethering complex uses its two Rab bindings to determine the place of SNARE assembly and thus fusion at endomembranes.

MeSH terms

  • Binding Sites
  • Endosomes / metabolism
  • Membrane Fusion / physiology*
  • Phosphorylation
  • Protein Binding
  • Protein Transport / physiology
  • SNARE Proteins / metabolism
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Saccharomyces cerevisiae Proteins / physiology
  • Vacuoles / metabolism
  • Vesicular Transport Proteins / metabolism
  • rab GTP-Binding Proteins / metabolism*
  • rab GTP-Binding Proteins / physiology

Substances

  • SNARE Proteins
  • Saccharomyces cerevisiae Proteins
  • Vesicular Transport Proteins
  • YPT7 protein, S cerevisiae
  • rab GTP-Binding Proteins