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剖析M3毒蕈碱型乙酰胆碱受体保守的NPxxY基序:Asp-7.49在受体信号传导和多蛋白复合物形成中的关键作用

Dissecting the conserved NPxxY motif of the M3 muscarinic acetylcholine receptor: critical role of Asp-7.49 for receptor signaling and multiprotein complex formation.

作者信息

Borroto-Escuela Dasiel O, Romero-Fernandez Wilber, García-Negredo Gloria, Correia Patricia A, Garriga Pere, Fuxe Kjell, Ciruela Francisco

机构信息

Centre de Biotecnologia Molecular, Department d'Enginyeria Quémica, Universitat Politècnica de Catalunya, Terrassa, Spain.

出版信息

Cell Physiol Biochem. 2011;28(5):1009-22. doi: 10.1159/000335788. Epub 2011 Dec 15.

DOI:10.1159/000335788
PMID:22178951
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 Gα(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 M(3)R and ARF1 and also for the formation of the ARF/Rho/β γ 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.

摘要

乙酰胆碱刺激可导致M(3)毒蕈碱型乙酰胆碱受体激活,并使辅助/支架蛋白募集到信号体复合物中。这种复合物的动力学尚未完全了解,但发现位于受体跨膜7区和近膜螺旋8区内的保守NPxxY基序可调节G蛋白激活。在此,我们通过受体诱变揭示了保守的M(3)毒蕈碱型乙酰胆碱受体NPxxY基序在配体结合、信号传导和多蛋白复合物形成中的作用。有趣的是,虽然N7.49D受体突变体表现出正常的配体结合特性,但N7.49A突变体的拮抗剂结合减少,对卡巴胆碱的亲和力增加。此外,除了最后一个突变体在卡巴胆碱刺激后能够与Gα(q/11)发生物理偶联外,它既不能激活磷脂酶C也不能激活磷脂酶D。另一方面,我们证明Asn-7.49对于M(3)R与ARF1之间的相互作用以及ARF/Rho/βγ信号复合物的形成很重要,该复合物可能决定PLD的快速激活和脱敏。总体而言,这些结果表明M(3)毒蕈碱型乙酰胆碱受体的NPxxY基序作为受体信号传导和多蛋白复合物形成的关键构象开关。

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