Domazet Ivana, Holleran Brian J, Martin Stéphane S, Lavigne Pierre, Leduc Richard, Escher Emanuel, Guillemette Gaétan
Department of Pharmacology, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, Quebec J1H 5N4, Canada.
J Biol Chem. 2009 May 1;284(18):11922-9. doi: 10.1074/jbc.M808113200. Epub 2009 Mar 9.
The octapeptide hormone angiotensin II (AngII) exerts a wide variety of cardiovascular effects through the activation of the angiotensin II type-1 (AT(1)) receptor, which belongs to the G protein-coupled receptor superfamily. Like other G protein-coupled receptors, the AT(1) receptor possesses seven transmembrane domains that provide structural support for the formation of the ligand-binding pocket. In order to identify those residues in the second transmembrane domain (TMD2) that contribute to the formation of the binding pocket of the AT(1) receptor, we used the substituted cysteine accessibility method. All of the residues within the Leu-70 to Trp-94 region were mutated one at a time to a cysteine, and, after expression in COS-7 cells, the mutant receptors were treated with the sulfhydryl-specific alkylating agent methanethiosulfonate-ethylammonium (MTSEA). MTSEA reacts selectively with water-accessible, free sulfhydryl groups of endogenous or introduced point mutation cysteines. If a cysteine is found in the binding pocket, the covalent modification will affect the binding kinetics of the ligand. MTSEA substantially decreased the binding affinity of D74C-AT(1), L81C-AT(1), A85C-AT(1), T88C-AT(1), and A89C-AT(1) mutant receptors, which suggests that these residues orient themselves within the water-accessible binding pocket of the AT(1) receptor. Interestingly, this pattern of acquired MTSEA sensitivity was altered for TMD2 reporter cysteines engineered in a constitutively active N111G-AT(1) receptor background. Indeed, mutant D74C-N111G-AT(1) became insensitive to MTSEA, whereas mutant L81C-N111G-AT(1) lost some sensitivity and mutant V86C-N111G-AT(1) became sensitive to MTSEA. Our results suggest that constitutive activation of the AT(1) receptor causes TMD2 to pivot, bringing the top of TMD2 closer to the binding pocket and pushing the bottom of TMD2 away from the binding pocket.
八肽激素血管紧张素II(AngII)通过激活血管紧张素II 1型(AT(1))受体发挥多种心血管效应,该受体属于G蛋白偶联受体超家族。与其他G蛋白偶联受体一样,AT(1)受体具有七个跨膜结构域,为配体结合口袋的形成提供结构支持。为了确定第二跨膜结构域(TMD2)中有助于形成AT(1)受体结合口袋的那些残基,我们使用了半胱氨酸替代可及性方法。将Leu-70至Trp-94区域内的所有残基逐一突变为半胱氨酸,在COS-7细胞中表达后,用巯基特异性烷基化剂甲硫代磺酸乙酯铵(MTSEA)处理突变受体。MTSEA与内源性或引入的点突变半胱氨酸的可及水相游离巯基选择性反应。如果在结合口袋中发现半胱氨酸,共价修饰将影响配体的结合动力学。MTSEA显著降低了D74C-AT(1)、L81C-AT(1)、A85C-AT(1)、T88C-AT(1)和A89C-AT(1)突变受体的结合亲和力,这表明这些残基定位于AT(1)受体的可及水相结合口袋内。有趣的是,在组成型活性N111G-AT(1)受体背景中构建的TMD2报告半胱氨酸的这种获得性MTSEA敏感性模式发生了改变。实际上,突变体D74C-N111G-AT(1)对MTSEA变得不敏感,而突变体L81C-N111G-AT(1)失去了一些敏感性,突变体V86C-N111G-AT(1)对MTSEA变得敏感。我们的结果表明,AT(1)受体的组成型激活导致TMD2发生枢转,使TMD2的顶部更靠近结合口袋,并将TMD2的底部推离结合口袋。