Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/126278
Title: Dissecting the conserved NPxxY motif of the M<sub>3</sub> muscarinic acetylcholine receptor: critical role of Asp-7.49 for receptor signaling and multiprotein complex formation
Author: Borroto Escuela, Dasiel Oscar
Romero Fernández, Wilber
García Negredo, Gloria
Correia, Patricia A.
Garriga, Pere
Fuxe, Kjell
Ciruela Alférez, Francisco
Keywords: Proteïnes G
Receptors colinèrgics
G Proteins
Acetylcholine receptors
Issue Date: 15-Dec-2011
Publisher: Karger
Abstract: Acetylcholine challenge produces M-3 muscarinic acetylcholine receptor activation and accessory/scaffold proteins recruitment into a signalsome complex. The dynamics of such a complex is not well understood but a conserved NPxxY motif located within transmembrane 7 and juxtamembrane helix 8 of the receptor was found to modulate G protein activation. Here by means of receptor mutagenesis we unravel the role of the conserved M-3 muscarinic acetylcholine receptor NPxxY motif on ligand binding, signaling and multiprotein complex formation. Interestingly, while a N7.49D receptor mutant showed normal ligand binding properties a N7.49A mutant had reduced antagonist binding and increased affinity for carbachol. Also, besides this last mutant was able to physically couple to G alpha(q/11) after carbachol challenge it was neither capable to activate phospholipase C nor phospholipase D. On the other hand, we demonstrated that the Asn-7.49 is important for the interaction between M3R and ARF1 and also for the formation of the ARF/Rho/beta gamma signaling complex, a complex that might determine the rapid activation and desensitization of PLD. Overall, these results indicate that the NPxxY motif of the M-3 muscarinic acetylcholine receptor acts as key conformational switch for receptor signaling and multiprotein complex formation.
Note: Reproducció del document publicat a: https://doi.org/10.1159/000335788
It is part of: Cellular Physiology and Biochemistry, 2011, vol. 28, num. 5, p. 1009-1022
URI: http://hdl.handle.net/2445/126278
Related resource: https://doi.org/10.1159/000335788
ISSN: 1015-8987
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Patologia i Terapèutica Experimental)

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