2022Nature CommunicationsOpen access

The dopamine transporter antiports potassium to increase the uptake of dopamine

Solveig Gaarde Schmidt, Mette Galsgaard Malle, Anne Kathrine Nielsen, Søren S.-R. Bohr, Ciara Frances Pugh, Jeppe C. Nielsen, Ida H. Poulsen, Kasper Dyrberg Rand, Nikos S. Hatzakis, Claus Juul Loland

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Abstract

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.

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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.

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Available abstract

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.

Key concepts: Dopamine, Dopamine transporter, Transporter, Potassium, Dopamine Plasma Membrane Transport Proteins, Chemistry, Biology, Neuroscience

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