Institute of Pharmacology & Toxicology, University of Würzburg, 97078 Würzburg, Germany.
J Biol Chem. 2010 Mar 12;285(11):8227-33. doi: 10.1074/jbc.M109.015388. Epub 2010 Jan 14.
Active G protein-coupled receptors activate heterotrimeric Galphabetagamma proteins by catalyzing the exchange of GDP by GTP at the Galpha subunit. A paradoxical attenuation of G protein-activated inwardly rectifying potassium channels (GIRK) upon stimulation of native cells with high concentrations of agonist is known. However, a deactivation of activated G proteins by active receptors has not been experimentally studied in intact cells. We monitored GIRK currents and G(o) protein activation by means of fluorescence resonance energy transfer (FRET) in parallel. The results suggested that GIRK currents were paradoxically attenuated due to an inactivation of G(o) proteins by active alpha(2A)-adrenergic receptors. To study the mechanisms, G protein activation and receptor-G protein interactions were analyzed as a function of nucleotide type and nucleotide concentrations by means of FRET, while controlling intracellular nucleotides upon permeabilization of the cell membrane. Results suggested a receptor-catalyzed dissociation of GTP from activated heterotrimeric Galphabetagamma. Consequently, nucleotide-free G proteins were sequestrated in heterotrimeric conformation at the active receptor, thus attenuating downstream signaling in an agonist-dependent manner.
活性 G 蛋白偶联受体通过催化 Galpha 亚基上 GDP 与 GTP 的交换,激活异三聚体 Galpha beta gamma 蛋白。已知在刺激天然细胞时,高浓度激动剂会使 G 蛋白激活的内向整流钾通道(GIRK)产生矛盾性的衰减。然而,在完整细胞中,活性受体对激活的 G 蛋白的失活尚未进行实验研究。我们通过荧光共振能量转移(FRET)平行监测 GIRK 电流和 G(o) 蛋白的激活。结果表明,由于活性 alpha(2A)-肾上腺素能受体使 G(o) 蛋白失活,GIRK 电流出现矛盾性衰减。为了研究机制,我们通过 FRET 分析了 G 蛋白的激活和受体-G 蛋白相互作用作为核苷酸类型和核苷酸浓度的函数,同时在细胞膜通透化时控制细胞内核苷酸。结果表明,受体催化激活的异三聚体 Galpha beta gamma 中的 GTP 从 G 蛋白解离。因此,无核苷酸的 G 蛋白以三聚体构象在活性受体中被隔离,从而以激动剂依赖的方式减弱下游信号转导。