Division of Medicinal Chemistry, Leiden/Amsterdam Centre for Drug Research, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands.
FASEB J. 2011 Feb;25(2):632-43. doi: 10.1096/fj.10-164319. Epub 2010 Oct 28.
The highly variable extracellular loops in G protein-coupled receptors (GPCRs) have been implicated in receptor activation, the mechanism of which is poorly understood. In a random mutagenesis screen on the human adenosine A(2B) receptor (A(2B)R) using the MMY24 Saccharomyces cerevisiae strain as a read-out system, we found that two residues in the first extracellular loop, a phenylalanine and an aspartic acid at positions 71 and 74, respectively, are involved in receptor activation. We subsequently performed further site-directed and site-saturation mutagenesis. These experiments revealed that the introduction of mutations at either of the identified positions results in a wide variety of receptor activation profiles, with changes in agonist potency, constitutive activity, and intrinsic activity. Radioligand binding studies showed that the changes in activation were not due to changes in receptor expression. We interpret these data in the light of the recently revealed structure of the adenosine A(2A)R, the closest homologue of the A(2B)R. The two residues are suggested to be vital in maintaining the tertiary structure of a β sheet in the extracellular domain of the A(2B)R. We hypothesize that deterioration of structure in the extracellular domains of GPCRs compromises overall receptor structure with profound consequences for receptor activation and constitutive activity.
G 蛋白偶联受体 (GPCR) 的高度可变细胞外环与受体激活有关,但这一机制尚未完全了解。我们使用 MMY24 酿酒酵母菌株作为读出系统,对人腺苷 A(2B)受体 (A(2B)R) 进行随机诱变筛选,发现第一个细胞外环中的两个残基,第 71 位和第 74 位的苯丙氨酸和天冬氨酸,参与了受体的激活。随后,我们进行了进一步的定点和定点饱和诱变。这些实验表明,在鉴定出的位置之一引入突变会导致受体激活谱的广泛变化,包括激动剂效力、组成性活性和内在活性的变化。放射性配体结合研究表明,激活的变化不是由于受体表达的变化引起的。我们根据最近揭示的腺苷 A(2A)R 结构(与 A(2B)R 最接近的同源物)来解释这些数据。这两个残基被认为对维持 A(2B)R 细胞外环中β片层的三级结构至关重要。我们假设 GPCR 细胞外环结构的恶化会破坏整体受体结构,对受体激活和组成性活性产生深远影响。