Novel Inhibitory Site Revealed by XAP044 Mode of Action on the Metabotropic Glutamate 7 Receptor Venus Flytrap Domain

Cristiano, Nunzia and Cabaye, Alexandre and Brabet, Isabelle and Glatthar, Ralf and Tora, Amelie and Goudet, Cyril and Bertrand, Hugues-Olivier and Goupil-Lamy, Anne and Flor, Peter J. and Pin, Jean-Philippe and McCort-Tranchepain, Isabelle and Acher, Francine C. (2024) Novel Inhibitory Site Revealed by XAP044 Mode of Action on the Metabotropic Glutamate 7 Receptor Venus Flytrap Domain. JOURNAL OF MEDICINAL CHEMISTRY, 67 (14). pp. 11662-11687. ISSN 0022-2623, 1520-4804

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Abstract

Metabotropic glutamate (mGlu) receptors play a key role in modulating most synapses in the brain. The mGlu7 receptors inhibit presynaptic neurotransmitter release and offer therapeutic possibilities for post-traumatic stress disorders or epilepsy. Screening campaigns provided mGlu7-specific allosteric modulators as the inhibitor XAP044 (Gee et al. J. Biol. Chem. 2014). In contrast to other mGlu receptor allosteric modulators, XAP044 does not bind in the transmembrane domain but to the extracellular domain of the mGlu7 receptor and not at the orthosteric site. Here, we identified the mode of action of XAP044, combining synthesis of derivatives, modeling and docking experiments, and mutagenesis. We propose a unique mode of action of these inhibitors, preventing the closure of the Venus flytrap agonist binding domain. While acting as a noncompetitive antagonist of L-AP4, XAP044 and derivatives act as apparent competitive antagonists of LSP4-2022. These data revealed more potent XAP044 analogues and new possibilities to target mGluRs.

Item Type: Article
Uncontrolled Keywords: ALLOSTERIC MODULATOR; MOLECULAR-BASIS; IN-VITRO; ACTIVATION; BINDING; STRESS; VALIDATION; MEMBRANES; POTENCY; AGONIST;
Subjects: 500 Science > 570 Life sciences
Divisions: Biology, Preclinical Medicine > Institut für Zoologie > Molecular and Cellular Neurobiology (Prof. Dr. Peter J. Flor)
Depositing User: Dr. Gernot Deinzer
Date Deposited: 15 Jan 2026 14:27
Last Modified: 15 Jan 2026 14:27
URI: https://pred.uni-regensburg.de/id/eprint/65253

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