Department of Physiology, UCSF School of Medicine, San Francisco, United States; Department of Neurology, UCSF School of Medicine, San Francisco, United States; Graduate Program in Biomedical Sciences, UCSF School of Medicine, San Francisco, United States
Department of Physiology, UCSF School of Medicine, San Francisco, United States; Department of Neurology, UCSF School of Medicine, San Francisco, United States
Department of Physiology, UCSF School of Medicine, San Francisco, United States; Department of Neurology, UCSF School of Medicine, San Francisco, United States; Graduate Program in Biomedical Sciences, UCSF School of Medicine, San Francisco, United States; Kavli Institute for Fundamental Neuroscience, UCSF School of Medicine, San Francisco, United States; Weill Institute for Neurosciences, UCSF School of Medicine, San Francisco, United States
The transport of glutamate into synaptic vesicles exhibits an unusual form of regulation by Cl- as well as an associated Cl- conductance. To distinguish direct effects of Cl- on the transporter from indirect effects via the driving force Δψ, we used whole endosome recording and report the first currents due to glutamate flux by the vesicular glutamate transporters (VGLUTs). Chloride allosterically activates the VGLUTs from both sides of the membrane, and we find that neutralization of an arginine in transmembrane domain four suffices for the lumenal activation. The dose dependence suggests that Cl- permeates through a channel and glutamate through a transporter. Competition between the anions nonetheless indicates that they use a similar permeation pathway. By controlling both ionic gradients and Δψ, endosome recording isolates different steps in the process of synaptic vesicle filling, suggesting distinct roles for Cl- in both allosteric activation and permeation.