Allosteric modulation of proton binding confers Cl- activation and glutamate selectivity to vesicular glutamate transporters

Abstract

Vesicular glutamate transporters (VGLUTs) fill synaptic vesicles with glutamate and remove luminal Cl^- via an additional anion channel mode. Both of these transport functions are stimulated by luminal acidification, luminal-positive membrane potential, and luminal Cl^-. We studied VGLUT1 transporter/channel activation using a combination of heterologous expression, cellular electrophysiology, fast solution exchange, and mathematical modeling. Cl^- channel gating can be described with a kinetic scheme that includes two protonation sites and distinct opening, closing, and Cl^--binding rates for each protonation state. Cl^- binding promotes channel opening by modifying the pKa values of the protonation sites and rates of pore opening and closure. VGLUT1 transports glutamate and aspartate at distinct stoichiometries: H⁺-glutamate exchange at 1:1 stoichiometry and aspartate uniport. Neurotransmitter transport with variable stoichiometry can be described with an alternating access model that assumes that transporters without substrate translocate in the doubly protonated state to the inward-facing conformation and return with the bound amino acid substrate as either singly or doubly protonated. Glutamate, but not aspartate, promotes the release of one proton from inward-facing VGLUT1, resulting in preferential H⁺-coupled glutamate exchange. Cl^- stimulates glutamate transport by making the glutamate-binding site accessible to cytoplasmic glutamate and by facilitating transitions to the inward-facing conformation after outward substrate release. We conclude that allosteric modification of transporter protonation by Cl^- is crucial for both VGLUT1 transport functions.