Feng Y H, Miura S, Husain A, Karnik S S
Department of Molecular Cardiology, Research Institute, The Cleveland Clinic Foundation, Ohio 44195, USA.
Biochemistry. 1998 Nov 10;37(45):15791-8. doi: 10.1021/bi980863t.
The AT1 receptor is a G-protein-coupled receptor (GPCR); its activation from the basal state (R) requires an interaction between Asn111 in transmembrane helix III (TM-III) of the receptor and the Tyr4 residue of angiotensin II (Ang II). Asn111 to Gly111 mutation (N111G) results in constitutive activation of the AT1 receptor (Noda et al. (1996) Biochemistry, 35, 16435-16442). We show here that replacement of the AT1 receptors TM-III with a topologically identical 16-residue segment (Cys101-Val116) from the AT2 receptor induces constitutive activity, although Asn111 is preserved in the resulting chimera, CR18. Effects of CR18 and N111G mutations are neither additive nor synergistic. The conformation(s) induced in either mutant mimics the partially activated state (R'), and transition to the fully activated R conformation in both no longer requires the Tyr4 of Ang II. Both the R state of the receptor and the Tyr4 Ang II dependence of receptor activation can be reinstated by introduction of a larger sized Phe side chain at the 111 position in CR18, suggesting that the CR18 mutation generated an effect similar to the reduction of side chain size in the N111G mutation. Consistently in the native AT1 receptor, R' conformation is generated by replacement with residues smaller but not larger than the Asn111. However, size substitution of several other TM-III residues in both receptors did not affect transitions between R, R', and R states. Thus, the property responsible for Asn111 function as a conformational switch is neither polarity nor hydrogen bonding potential but the side chain size. We conclude that the fundamental mechanism responsible for constitutive activation of the AT1 receptor is to increase the entropy of the key agonist-switch binding residue, Asn111. As a result, the normally agonist-dependent R --> R' transition occurs spontaneously. This mechanism may be applicable to many other GPCRs.
AT1受体是一种G蛋白偶联受体(GPCR);其从基础状态(R)的激活需要受体跨膜螺旋III(TM-III)中的Asn111与血管紧张素II(Ang II)的Tyr4残基之间相互作用。Asn111突变为Gly111(N111G)会导致AT1受体的组成性激活(野田等人,《生物化学》,1996年,第35卷,第16435 - 16442页)。我们在此表明,用来自AT2受体的拓扑结构相同的16个残基片段(Cys101 - Val116)替换AT1受体的TM-III会诱导组成性活性,尽管在所得嵌合体CR18中Asn111得以保留。CR18和N111G突变的效应既非相加也非协同。在任一突变体中诱导的构象模拟部分激活状态(R'),并且在两者中向完全激活的R构象的转变不再需要Ang II的Tyr4。通过在CR18的111位引入更大尺寸的苯丙氨酸侧链,可以恢复受体的R状态以及受体激活对Tyr4 Ang II的依赖性,这表明CR18突变产生的效应类似于N111G突变中侧链尺寸的减小。在天然AT1受体中同样如此,用小于但不大于Asn111的残基替换会产生R'构象。然而,在两个受体中对其他几个TM-III残基进行尺寸替换并不影响R态与R'态之间的转变。因此,Asn111作为构象开关发挥功能所依赖的特性既不是极性也不是氢键潜力,而是侧链尺寸。我们得出结论,AT1受体组成性激活的基本机制是增加关键激动剂 - 开关结合残基Asn111的熵。结果,通常依赖激动剂的R→R'转变会自发发生。这种机制可能适用于许多其他GPCR。