ACS Medicinal Chemistry Letters · 2015 · 11 citations · 34 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryMolecular PharmacologyNeuropharmacologyDrug-receptor InteractionsLigand BindingNeurotransmitter ReceptorsReceptor BindingReceptor PharmacologyReceptor-ligand InteractionsAgonist ActivityDopamine Receptor AgonistsDopamine Receptor SignalingDopamine Receptor SubtypesG-protein-coupled ReceptorsMembrane Receptor ActivationMembrane Receptor PharmacologyReceptor-ligand Structural Biology
Peptide nucleic acid scaffolds represent a promising tool to interrogate the multivalent effects of ligand binding to a membrane receptor. Dopamine D2 receptors (D2R) are a class of G-protein coupled receptors (GPCRs), and the formation of higher-ordered structures of these receptors has been associated with the progression of several neurological diseases. In this Letter, we describe the synthesis of a library of ligand-modified PNAs bearing a known D2R agonist, (±)-PPHT. The D2R activity for each construct was assessed, and the multivalent effects were evaluated.
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PNA hybridizes to complementary oligonucleotides obeying the Watson–Crick hydrogen-bonding rules
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