| Literature DB >> 29642010 |
Julia Preobraschenski1, Cyril Cheret2, Marcelo Ganzella1, Johannes Friedrich Zander2, Karin Richter2, Stephan Schenck3, Reinhard Jahn4, Gudrun Ahnert-Hilger5.
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.Entities:
Keywords: ATPase; SLC17 family; VGLUT; anti-VGLUT1 nanobody; hybrid vesicles; proteoliposomes; type I Na(+)-dependent inorganic phosphate transporter
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Year: 2018 PMID: 29642010 DOI: 10.1016/j.celrep.2018.03.055
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423