Generation of an Activating Zn2+Switch in the Dopamine Transporter: Mutation of an Intracellular Tyrosine Constitutively Alters the Conformational Equilibrium of the Transport Cycle

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 99; no. 3; pp. 1683 - 1688
• Main Authors: Loland, Claus Juul, Norregaard, Lene, Litman, Thomas, Gether, Ulrik
• Format: Journal Article
• Language: English
• Published: National Academy of Sciences 05.02.2002; National Acad Sciences; The National Academy of Sciences
• Subjects: Binding sites; Biological Sciences; Cocaine; COS cells; Dopamine plasma membrane transport proteins; Experimental procedures; Neuroscience; Phenotypes; Receptors; Serotonin plasma membrane transport proteins; Sodium
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.032386299

Binding of Zn2+to the endogenous Zn2+binding site in the human dopamine transporter leads to potent inhibition of [3H]dopamine uptake. Here we show that mutation of an intracellular tyrosine to alanine (Y335A) converts this inhibitory Zn2+switch into an activating Zn2+switch, allowing Zn2+-dependent activation of the transporter. The tyrosine is part of a conserved YXXΦ trafficking motif (X is any residue and Φ is a residue with a bulky hydrophobic group), but Y335A did not show alterations in surface targeting or protein kinase C-mediated internalization. Despite wild-type levels of surface expression, Y335A displayed a dramatic decrease in [3H]dopamine uptake velocity (Vmax) to less than 1% of the wild type. In addition, Y335A showed up to 150-fold decreases in the apparent affinity for cocaine, mazindol, and related inhibitors whereas the apparent affinity for several substrates was increased. However, the presence of Zn2+in micromolar concentrations increased the Vmaxup to 24-fold and partially restored the apparent affinities. The capability of Zn2+to restore transport is consistent with a reversible, constitutive shift in the distribution of conformational states in the transport cycle upon mutation of Tyr-335. We propose that this shift is caused by disruption of intramolecular interactions important for stabilizing the transporter in a conformation in which extracellular substrate can bind and initiate transport, and accordingly that Tyr-335 is critical for regulating isomerization between discrete states in the transport cycle.