Abstract
The dopamine transporter facilitates dopamine reuptake from the extracellular space to terminate neurotransmission. The transporter belongs to the neurotransmitter:sodium symporter family, which includes transporters for serotonin, norepinephrine, and GABA that utilize the Na+ gradient to drive the uptake of substrate. Decades ago, it was shown that the serotonin transporter also antiports K+, but investigations of K+-coupled transport in other neurotransmitter:sodium symporters have been inconclusive. Here, we show that ligand binding to the Drosophila- and human dopamine transporters are inhibited by K+, and the conformational dynamics of the Drosophila dopamine transporter in K+ are divergent from the apo- and Na+-states. Furthermore, we find that K+ increases dopamine uptake by the Drosophila dopamine transporter in liposomes, and visualize Na+ and K+ fluxes in single proteoliposomes using fluorescent ion indicators. Our results expand on the fundamentals of dopamine transport and prompt a reevaluation of the impact of K+ on other transporters in this pharmacologically important family.
Original language | English |
---|---|
Article number | 2446 |
Journal | Nature Communications |
Volume | 13 |
Issue number | 1 |
Number of pages | 12 |
ISSN | 2041-1723 |
DOIs | |
Publication status | Published - 2022 |
Bibliographical note
© 2022. The Author(s).Keywords
- Animals
- Dopamine/metabolism
- Dopamine Plasma Membrane Transport Proteins/metabolism
- Drosophila/metabolism
- Ion Transport
- Ions/metabolism
- Neurotransmitter Agents/metabolism
- Potassium/metabolism
- Serotonin Plasma Membrane Transport Proteins/metabolism
- Sodium/metabolism
- Symporters/metabolism