Structure-based discovery of conformationally selective inhibitors of the serotonin transporter
Cell(2023)
Abstract
The serotonin transporter (SERT) removes synaptic serotonin and is the target of anti-depressant drugs. SERT adopts three conformations: outward-open, occluded, and inward-open. All known inhibitors target the outward-open state except ibogaine, which has unusual anti-depressant and substance-withdrawal ef-fects, and stabilizes the inward-open conformation. Unfortunately, ibogaine's promiscuity and cardiotoxicity limit the understanding of inward-open state ligands. We docked over 200 million small molecules against the inward-open state of the SERT. Thirty-six top-ranking compounds were synthesized, and thirteen inhibited; further structure-based optimization led to the selection of two potent (low nanomolar) inhibitors. These sta-bilized an outward-closed state of the SERT with little activity against common off-targets. A cryo-EM struc-ture of one of these bound to the SERT confirmed the predicted geometry. In mouse behavioral assays, both compounds had anxiolytic-and anti-depressant-like activity, with potencies up to 200-fold better than fluox-etine (Prozac), and one substantially reversed morphine withdrawal effects.
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