Valant Celine, Gregory Karen J, Hall Nathan E, Scammells Peter J, Lew Michael J, Sexton Patrick M, Christopoulos Arthur
Drug Discovery Biology Laboratory, Monash University, 3800 Victoria, Australia.
J Biol Chem. 2008 Oct 24;283(43):29312-21. doi: 10.1074/jbc.M803801200. Epub 2008 Aug 22.
Many G protein-coupled receptors (GPCRs) possess allosteric binding sites distinct from the orthosteric site utilized by their cognate ligands, but most GPCR allosteric modulators reported to date lack signaling efficacy in their own right. McN-A-343 (4-(N-(3-chlorophenyl)carbamoyloxy)-2-butynyltrimethylammonium chloride) is a functionally selective muscarinic acetylcholine receptor (mAChR) partial agonist that can also interact allosterically at the M(2) mAChR. We hypothesized that this molecule simultaneously utilizes both an allosteric and the orthosteric site on the M(2) mAChR to mediate these effects. By synthesizing progressively truncated McN-A-343 derivatives, we identified two, which minimally contain 3-chlorophenylcarbamate, as pure allosteric modulators. These compounds were positive modulators of the orthosteric antagonist N-[(3)H]methylscopolamine, but in functional assays of M(2) mAChR-mediated ERK1/2 phosphorylation and guanosine 5'-3-O-([(35)S]thio)triphosphate binding, they were negative modulators of agonist efficacy. This negative allosteric effect was diminished upon mutation of Y177A in the second extracellular (E2) loop of the M(2) mAChR that is known to reduce prototypical allosteric modulator potency. Our results are consistent with McN-A-343 being a bitopic orthosteric/allosteric ligand with the allosteric moiety engendering partial agonism and functional selectivity. This finding suggests a novel and largely unappreciated mechanism of "directed efficacy" whereby functional selectivity may be engendered in a GPCR by utilizing an allosteric ligand to direct the signaling of an orthosteric ligand encoded within the same molecule.
许多G蛋白偶联受体(GPCR)具有与同源配体所利用的正构位点不同的别构结合位点,但迄今为止报道的大多数GPCR别构调节剂本身缺乏信号传导效力。McN-A-343(4-(N-(3-氯苯基)氨基甲酰氧基)-2-丁炔基三甲基氯化铵)是一种功能选择性毒蕈碱型乙酰胆碱受体(mAChR)部分激动剂,它也可以在M(2) mAChR上进行别构相互作用。我们假设该分子同时利用M(2) mAChR上的别构位点和正构位点来介导这些效应。通过逐步合成截短的McN-A-343衍生物,我们鉴定出两种最少含有3-氯苯基氨基甲酸酯的化合物作为纯别构调节剂。这些化合物是正构拮抗剂N-[(3)H]甲基东莨菪碱的正性调节剂,但在M(2) mAChR介导的ERK1/2磷酸化和鸟苷5'-3-O-([(35)S]硫代)三磷酸结合的功能测定中,它们是激动剂效力的负性调节剂。当M(2) mAChR的第二个细胞外环(E2)中的Y177A发生突变时,这种负性别构效应减弱,已知该突变会降低典型别构调节剂的效力。我们的结果与McN-A-343是一种双位点正构/别构配体一致,其中别构部分产生部分激动作用和功能选择性。这一发现提示了一种新颖且在很大程度上未被认识的“定向效力”机制,即通过利用别构配体来引导同一分子内编码的正构配体的信号传导,从而在GPCR中产生功能选择性。