Insights into the cholecystokinin 2 receptor binding site and processes of activation.

Michaël Paillasse 1 Céline Deraeve 2 Philippe De Medina 1, 2 Loubna Mhamdi 2 Gilles Favre 2 Marc Poirot 2 Sandrine Silvente-Poirot 2
1 Affichem
2 Departement /u563 : Oncogenèse, Signalisation et Innovation thérapeutique
Centre de Physiopathologie Toulouse Purpan (ex IFR 30 et IFR 150), Institut Claudius Regaud
Abstract : The cholecystokinin (CCK) 2 receptor (CCK2R) appears as a pharmacological target for the treatment of many major diseases. To complete the mapping of the CCK2R binding site and its activation processes, we have looked for the receptor residues that interact with Trp6, an essential residue for CCK binding and activity. In our molecular model of the CCK-occupied CCK2R, the indole group of Trp6 stacked with the phenyl ring of Phe120 (ECL1) and interacted with the imidazole group of His381(H7.39) and the phenyl ring of Tyr385(H7.43). Mutagenesis and pharmacological studies validated these interactions. It is noteworthy that the mutation of Phe120 to Trp conferred constitutive activity to the CCK2R. Molecular modeling and experimental works identified the residues involved in the activation cascade initiated by Trp6 and revealed that the constitutively active F120W mutation mimics the conformational changes induced by Trp6 resulting in: 1) the exposure of Glu151(E3.49) of the conserved E/DRY motif 2) the formation of an amphiphatic pocket involving protonated Glu151(E3.49) and Leu330 (ICL3), and 3) the opening of the intracellular loops 2 and 3 and the release of Arg158 (ICL2). The R158A mutation was shown to affect inositol phosphate production, whereas the E151A and L330E mutations induced constitutive inositol phosphate production. Given that a constitutively active variant of the CCK2R has been identified in different cancers and the fact that the E151A mutant has been reported to induce tumors, these studies should help in the development of potent inverse agonists to inhibit the constitutive activation of the CCK2R.
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Molecular Pharmacology, American Society for Pharmacology and Experimental Therapeutics, 2006, 70 (6), pp.1935-45. 〈10.1124/mol.106.029967〉
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http://www.hal.inserm.fr/inserm-00519168
Contributeur : Marc Poirot <>
Soumis le : samedi 18 septembre 2010 - 15:45:40
Dernière modification le : mardi 11 septembre 2018 - 16:20:02

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Michaël Paillasse, Céline Deraeve, Philippe De Medina, Loubna Mhamdi, Gilles Favre, et al.. Insights into the cholecystokinin 2 receptor binding site and processes of activation.. Molecular Pharmacology, American Society for Pharmacology and Experimental Therapeutics, 2006, 70 (6), pp.1935-45. 〈10.1124/mol.106.029967〉. 〈inserm-00519168〉

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