多巴胺
多巴胺转运体
运输机
钾
多巴胺质膜转运蛋白
化学
生物
神经科学
生物化学
多巴胺能
基因
有机化学
作者
Solveig G. Schmidt,Mette Galsgaard Malle,Anne Kathrine Nielsen,Søren S.-R. Bohr,Ciara Frances Pugh,Jeppe C. Nielsen,Ida H. Poulsen,Kasper D. Rand,Nikos S. Hatzakis,Claus J. Løland
标识
DOI:10.1038/s41467-022-30154-5
摘要
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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