Interrogating the Molecular Basis for Substrate Recognition in Serotonin and Dopamine Transporters with High-Affinity Substrate-Based Bivalent Ligands

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  • Jacob Andersen, University of Copenhagen
  • ,
  • Lucy Kate Ladefoged
  • Trine N. Bjerre Kristensen
  • ,
  • Lachlan Munro, University of Copenhagen
  • ,
  • Julie Grouleff
  • ,
  • Nicolai Stuhr-Hansen, University of Copenhagen
  • ,
  • Anders S. Kristensen, University of Copenhagen, Denmark
  • Birgit Schiott
  • Kristian Strømgaard, University of Copenhagen, Denmark

The transporters for the neurotransmitters serotonin and dopamine (SERT and DAT, respectively) are targets for drugs used in the treatment of mental disorders and widely used drugs of abuse. Studies of prokaryotic homologues have advanced our structural understanding of SERT and DAT, but it still remains enigmatic whether the human transporters contain one or two high-affinity substrate binding sites. We have designed and employed 24 bivalent ligands possessing a highly systematic combination of substrate moieties (serotonin and/or dopamine) and aliphatic or poly(ethylene glycol) spacers to reveal insight into substrate recognition in SERT and DAT. An optimized bivalent ligand comprising two serotonin moieties binds SERT with 3,800-fold increased affinity compared to that of serotonin, suggesting that the human transporters have two distinct substrate binding sites. We show that the bivalent ligands are inhibitors of SERT and an experimentally validated docking model suggests that the bivalent compounds bind with one substrate moiety in the central binding site (the Si site), whereas the other substrate moiety binds in a distinct binding site (the S2 site). A systematic study of nonconserved SERT/DAT residues surrounding the proposed binding region showed that nonconserved binding site residues do not contribute to selective recognition of substrates in SERT or DAT. This study provides novel insight into the molecular basis for substrate recognition in human transporters and provides an improved foundation for the development of new drugs targeting SERT and DAT.

Original languageEnglish
JournalACS Chemical Neuroscience
Volume7
Issue10
Pages (from-to)1406-1417
Number of pages12
ISSN1948-7193
DOIs
Publication statusPublished - Oct 2016

    Research areas

  • Serotonin transporter, dopamine transporter, alternating access mechanism, neurotransmitter transport, molecular pharmacology, induced-fit docking, NEUROTRANSMITTER-SODIUM SYMPORTER, ANTIDEPRESSANT BINDING-SITE, X-RAY STRUCTURES, REUPTAKE INHIBITORS, MONOAMINE TRANSPORTERS, S2 SITE, NOREPINEPHRINE TRANSPORTERS, BACTERIAL HOMOLOG, LEUT, MECHANISM

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