1. Academic Validation
  2. Dual and Direction-Selective Mechanisms of Phosphate Transport by the Vesicular Glutamate Transporter

Dual and Direction-Selective Mechanisms of Phosphate Transport by the Vesicular Glutamate Transporter

  • Cell Rep. 2018 Apr 10;23(2):535-545. doi: 10.1016/j.celrep.2018.03.055.
Julia Preobraschenski 1 Cyril Cheret 2 Marcelo Ganzella 1 Johannes Friedrich Zander 2 Karin Richter 2 Stephan Schenck 3 Reinhard Jahn 4 Gudrun Ahnert-Hilger 5
Affiliations

Affiliations

  • 1 Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • 2 Institute for Integrative Neuroanatomy, Charité, Medical University of Berlin, 10115 Berlin, Germany.
  • 3 Laboratory of Biomolecular Research, Paul Scherrer Institut, CH-5232 Villigen, Switzerland.
  • 4 Department of Neurobiology, Max-Planck-Institute for Biophysical Chemistry, 37077 Göttingen, Germany. Electronic address: rjahn@gwdg.de.
  • 5 Institute for Integrative Neuroanatomy, Charité, Medical University of Berlin, 10115 Berlin, Germany. Electronic address: gudrun.ahnert@charite.de.
Abstract

Vesicular glutamate transporters (VGLUTs) fill synaptic vesicles with glutamate and are thus essential for glutamatergic neurotransmission. However, VGLUTs were originally discovered as members of a transporter subfamily specific for inorganic phosphate (Pi). It is still unclear how VGLUTs accommodate glutamate transport coupled to an electrochemical proton gradient ΔμH+ with inversely directed Pi transport coupled to the Na+ gradient and the membrane potential. Using both functional reconstitution and heterologous expression, we show that VGLUT transports glutamate and Pi using a single substrate binding site but different coupling to cation gradients. When facing the cytoplasm, both ions are transported into synaptic vesicles in a ΔμH+-dependent fashion, with glutamate preferred over Pi. When facing the extracellular space, Pi is transported in a Na+-coupled manner, with glutamate competing for binding but at lower affinity. We conclude that VGLUTs have dual functions in both vesicle transmitter loading and Pi homeostasis within glutamatergic neurons.

Keywords

ATPase; SLC17 family; VGLUT; anti-VGLUT1 nanobody; hybrid vesicles; proteoliposomes; type I Na(+)-dependent inorganic phosphate transporter.

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