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Molecular basis of human GABA transporter 3 inhibition

Author

Listed:
  • Ravi Yadav

    (University of Southern California
    University of Southern California)

  • Gye Won Han

    (University of Southern California)

  • Cornelius Gati

    (University of Southern California
    University of Southern California
    University of Southern California)

Abstract

γ-Aminobutyric acid (GABA) transporters (GATs) are sodium- and chloride-dependent transporters that mediate the reuptake of the inhibitory neurotransmitter GABA after its release from synaptic vesicles. GAT3 transports GABA from the synaptic cleft into astrocytes and modulates synaptic signaling. GAT3 has been implicated in various neurological disorders and neurodegenerative diseases, rendering it a therapeutically important drug target. To understand the mechanism of transport and inhibition, here we determine cryo-electron microscopy structures of human GAT3 in its apo form and in complex with the selective inhibitor SNAP-5114. Unexpectedly, we have discovered that SNAP-5114 acts as a noncompetitive inhibitor at GAT3. SNAP-5114 binds at the orthosteric substrate binding pocket of GAT3 in its inward-open conformation, in agreement with its noncompetitive inhibition of GABA transport. In the apo state, GAT3 also adopts an inward-open conformation with the orthosteric substrate binding pocket exposed to cytoplasm, while an extensive network of interactions closes the extracellular gate. The structures, complemented with mutagenesis and radioligand uptake assays, show that the increased orthosteric substrate binding pocket volume and bulky moieties of SNAP-5114, drive the selective inhibition of GAT3 over GAT1. Our structural and functional studies reveal the mechanism of selective inhibition of GAT3 and provide a framework for GAT3-targeted rational drug design.

Suggested Citation

  • Ravi Yadav & Gye Won Han & Cornelius Gati, 2025. "Molecular basis of human GABA transporter 3 inhibition," Nature Communications, Nature, vol. 16(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59066-w
    DOI: 10.1038/s41467-025-59066-w
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    References listed on IDEAS

    as
    1. Zenia Motiwala & Nanda Gowtham Aduri & Hamidreza Shaye & Gye Won Han & Jordy Homing Lam & Vsevolod Katritch & Vadim Cherezov & Cornelius Gati, 2022. "Structural basis of GABA reuptake inhibition," Nature, Nature, vol. 606(7915), pages 820-826, June.
    2. Zenia Motiwala & Nanda Gowtham Aduri & Hamidreza Shaye & Gye Won Han & Jordy Homing Lam & Vsevolod Katritch & Vadim Cherezov & Cornelius Gati, 2022. "Publisher Correction: Structural basis of GABA reuptake inhibition," Nature, Nature, vol. 608(7921), pages 15-15, August.
    3. Atsuko Yamashita & Satinder K. Singh & Toshimitsu Kawate & Yan Jin & Eric Gouaux, 2005. "Crystal structure of a bacterial homologue of Na+/Cl--dependent neurotransmitter transporters," Nature, Nature, vol. 437(7056), pages 215-223, September.
    4. Azadeh Shahsavar & Peter Stohler & Gleb Bourenkov & Iwan Zimmermann & Martin Siegrist & Wolfgang Guba & Emmanuel Pinard & Steffen Sinning & Markus A. Seeger & Thomas R. Schneider & Roger J. P. Dawson , 2021. "Structural insights into the inhibition of glycine reuptake," Nature, Nature, vol. 591(7851), pages 677-681, March.
    5. Elia Zomot & Annie Bendahan & Matthias Quick & Yongfang Zhao & Jonathan A. Javitch & Baruch I. Kanner, 2007. "Mechanism of chloride interaction with neurotransmitter:sodium symporters," Nature, Nature, vol. 449(7163), pages 726-730, October.
    6. Per Plenge & Dongxue Yang & Kristine Salomon & Louise Laursen & Iris E. Kalenderoglou & Amy H. Newman & Eric Gouaux & Jonathan A. Coleman & Claus J. Loland, 2021. "The antidepressant drug vilazodone is an allosteric inhibitor of the serotonin transporter," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
    7. Kevin H. Wang & Aravind Penmatsa & Eric Gouaux, 2015. "Neurotransmitter and psychostimulant recognition by the dopamine transporter," Nature, Nature, vol. 521(7552), pages 322-327, May.
    8. Jonathan A. Coleman & Dongxue Yang & Zhiyu Zhao & Po-Chao Wen & Craig Yoshioka & Emad Tajkhorshid & Eric Gouaux, 2019. "Serotonin transporter–ibogaine complexes illuminate mechanisms of inhibition and transport," Nature, Nature, vol. 569(7754), pages 141-145, May.
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