The Role of Chloride Ions in Serotonin Transport
Abstract
The human serotonin transporter SERT facilitates serotonin (5-HT + ) transport into cells by coupling to Na + co-transport and K + exchange. Although extracellular Cl − is also essential for transport, whether Cl − ions are transported has been disputed, raising the question why Cl − ions are required? Here, we examine the role of Cl − using transport measurements, conformational assays, and molecular simulations. We show that Cl − is not transported and does not affect Na + -mediated cytoplasmic pathway closure but does reduce the accessibility of residues in the extracellular pathway, mimicking transport-related occlusion. Simulations indicate that Cl − ion binding constrains the helices in the so-called bundle, but not interactions spanning the extracellular pathway thought to act as a molecular gate. We surmise that Cl − (i) increases the stability of surrounding helices, (ii) enhances Na + binding affinity, and (iii) decreases extracellular pathway accessibility, thereby facilitating transport-related conformational changes. These findings explain SERT’s requirement for chloride and highlight distinct features of proteins in the same neurotransmitter transporter family.
Teaser
Decades-long question solved: Cl − ions boost serotonin reuptake by limiting transporter dynamics, not by crossing the membrane.
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