Identification of a small-molecule inhibitor of the PICK1 PDZ domain that inhibits hippocampal LTP and LTD

Research output: Contribution to journalJournal articleResearchpeer-review

Thor S Thorsen, Kenneth L Madsen, Nelson Rebola, Mette Rathje, Victor Anggono, Anders Bach, Irina S Moreira, Nicolai Stuhr-Hansen, Tino Dyhring, Dan Peters, Thijs Beuming, Richard Huganir, Harel Weinstein, Christophe Mulle, Kristian Strømgaard, Lars Christian B Rønn, Ulrik Gether

Proteins containing PSD-95/Discs-large/ZO-1 homology (PDZ) domains play key roles in the assembly and regulation of cellular signaling pathways and represent putative targets for new pharmacotherapeutics. Here we describe the first small-molecule inhibitor (FSC231) of the PDZ domain in protein interacting with C kinase 1 (PICK1) identified by a screening of approximately 44,000 compounds in a fluorescent polarization assay. The inhibitor bound the PICK1 PDZ domain with an affinity similar to that observed for endogenous peptide ligands (K(i) approximately 10.1 microM). Mutational analysis, together with computational docking of the compound in simulations starting from the PDZ domain structure, identified the binding mode of FSC231. The specificity of FSC231 for the PICK1 PDZ domain was supported by the lack of binding to PDZ domains of postsynaptic density protein 95 (PSD-95) and glutamate receptor interacting protein 1 (GRIP1). Pretreatment of cultured hippocampal neurons with FSC231 inhibited coimmunopreciptation of the AMPA receptor GluR2 subunit with PICK1. In agreement with inhibiting the role of PICK1 in GluR2 trafficking, FSC231 accelerated recycling of pHluorin-tagged GluR2 in hippocampal neurons after internalization in response to NMDA receptor activation. FSC231 blocked the expression of both long-term depression and long-term potentiation in hippocampal CA1 neurons from acute slices, consistent with inhibition of the bidirectional function of PICK1 in synaptic plasticity. Given the proposed role of the PICK1/AMPA receptor interaction in neuropathic pain, excitotoxicity, and cocaine addiction, FSC231 might serve as a lead in the future development of new therapeutics against these conditions.
Original languageEnglish
JournalProceedings of the National Academy of Science of the United States of America
Volume107
Issue number1
Pages (from-to)413-8
Number of pages5
ISSN0027-8424
DOIs
Publication statusPublished - 2010

Bibliographical note

Keywords: Animals; Binding Sites; COS Cells; Carbamates; Carrier Proteins; Cercopithecus aethiops; Cinnamates; Hippocampus; Humans; Long-Term Potentiation; Long-Term Synaptic Depression; Models, Molecular; Molecular Structure; Neuronal Plasticity; Neurons; Nuclear Proteins; PDZ Domains; Peptides; Protein Structure, Tertiary; Receptors, AMPA; Recombinant Fusion Proteins

ID: 21593465