Evaluation and Biological Properties of Reactive Ligands for the Mapping of the Glycine Site on the N-Methyl-d-aspartate (NMDA) Receptor

• Published in: Journal of medicinal chemistry 1999-10, Vol.42 (21), p.4394-4404
• Main Authors: Kreimeyer, Annett, Laube, Bodo, Sturgess, Mike, Goeldner, Maurice, Foucaud, Bernard
• Format: Article
• Language: English
• Subjects: Animals; Binding, Competitive; Biological and medical sciences; Brain - metabolism; Electrophysiology; Excitatory Amino Acid Antagonists - chemical synthesis; Excitatory Amino Acid Antagonists - chemistry; Excitatory Amino Acid Antagonists - metabolism; Excitatory Amino Acid Antagonists - pharmacology; Glutamatergic system (aspartate and other excitatory aminoacids); Glycine - pharmacology; In Vitro Techniques; Ligands; Medical sciences; Neuropharmacology; Neurotransmitters. Neurotransmission. Receptors; Oocytes; Pharmacology. Drug treatments; Quinolines - chemical synthesis; Quinolines - chemistry; Quinolines - metabolism; Quinolines - pharmacology; Radioligand Assay; Rats; Receptors, Glycine - biosynthesis; Receptors, Glycine - metabolism; Receptors, N-Methyl-D-Aspartate - biosynthesis; Receptors, N-Methyl-D-Aspartate - metabolism; Structure-Activity Relationship; Xenopus laevis
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm9910730

The glycine-binding site of the N-methyl-d-aspartate (NMDA) receptor, given its potential as pharmacological target, has been thoroughly studied by structure−activity relationships, which has made possible its description in terms of spatial limits and interactions of various types. A structural model, based on mutational analysis and sequence alignements, has been proposed. Yet, the amino acid residues responsible for the interactions with the ligand have not been unambiguously characterized. To evidence nucleophilic pocket-lining residues, we have designed and synthesized reactive glycine-site ligands derived from 3-substituted 4-hydroxy-quinolin-2(1H)-ones by introducing various electrophilic groups at different positions of the molecule. These ligands were found to have high affinity at the glycine site and to be functional antagonists by inhibiting glycine/glutamate-induced currents in transfected oocytes. The correlation between their potency and their substitution pattern was strictly consistent with previously established structure−activity relationships. Most ligands displayed intrinsic reactivity toward cysteine, but none inactivated wild-type receptors. This is consistent with the model since it indicates the absence of exposed cysteine in the glycine-binding site. A strategy of cysteine incorporation by point mutations at selected polypeptide positions will create unambiguously localized targets for our reactive probes.