Electrogenic Binding of Intracellular Cations Defines a Kinetic Decision Point in the Transport Cycle of the Human Serotonin Transporter.

The plasmalemmal monoamine transporters clear the extracellular space from their cognate substrates and sustain cellular monoamine stores even during neuronal activity. In some instances, however, the transporters enter a substrate-exchange mode, which results in release of intracellular substrate. Understanding what determines the switch between these two transport modes demands time-resolved measurements of intracellular (co-)substrate binding and release. Here, we report an electrophysiological investigation of intracellular solute-binding to the human serotonin transporter (SERT) expressed in HEK-293 cells. We measured currents induced by rapid application of serotonin employing varying intracellular (co-)substrate concentrations and interpreted the data using kinetic modeling. Our measurements revealed that the induction of the substrate-exchange mode depends on both voltage and intracellular Na(+) concentrations because intracellular Na(+) release occurs before serotonin release and is highly electrogenic. This voltage dependence was blunted by electrogenic binding of intracellular K(+) and, notably, also H(+) In addition, our data suggest that Cl(-) is bound to SERT during the entire catalytic cycle. Our experiments, therefore, document an essential role of electrogenic binding of K(+) or of H(+) to the inward-facing conformation of SERT in (i) cancelling out the electrogenic nature of intracellular Na(+) release and (ii) in selecting the forward-transport over the substrate-exchange mode. Finally, the kinetics of intracellular Na(+) release and K(+) (or H(+)) binding result in a voltage-independent rate-limiting step where SERT may return to the outward-facing state in a KCl- or HCl-bound form.