Im M J, Graham R M
Cellular and Molecular Research Laboratory, Massachusetts General Hospital, Boston.
J Biol Chem. 1990 Nov 5;265(31):18944-51.
The G-protein involved in alpha 1-adrenergic receptor signaling was identified using two different approaches. First, purified rat liver membranes were incubated with [alpha-32P]GTP in the absence or presence of the adrenergic agonist (-)-epinephrine, or in the presence of GTP. After UV irradiation, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and autoradiography, covalent labeling of a number of proteins was apparent and could be blocked by unlabeled GTP. In the preparation treated with (-)-epinephrine alone, labeling of a 74-kDa species was markedly enhanced. Enhanced labeling of 40-50-kDa species was also observed. Labeling of the 74-kDa protein was also evident in similarly treated membranes prepared from FRTL-5 thyroid cells, which contain abundant alpha 1-adrenergic receptors, but not in those prepared from turkey erythrocytes or NIH 3T3 fibroblasts, which are essentially devoid of alpha 1-receptors. Second, alpha 1-agonist-receptor-G-protein ternary complex formation was induced by incubating purified rat liver membranes with (-)-epinephrine. Rauwolscine (10(-7) M) and (+/-)-propranolol (10(-6) M) were included to prevent activation of alpha 2- and beta-adrenergic receptors by (-)-epinephrine. The ternary complex of hormone, receptor, and G-protein was solubilized, partially purified using heparin- and wheat germ agglutinin-agarose, and reconstituted into phospholipid vesicles. The vesicles displayed agonist-stimulated guanosine 5'-O-3-thiotriphosphate (GTP gamma S) binding that was blocked by phentolamine (10(-4) M). By contrast, stimulation of GTP gamma S binding was not evident when the vesicles were incubated with the beta-agonist, isoproterenol. Incubation of the vesicles with [alpha-32P]GTP or [alpha-32P]azido-GTP in the presence of (-)-epinephrine, followed by photolysis, sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and autoradiography, resulted in the covalent labeling of a 74-kDa protein. Labeling of this protein could be blocked by preincubation with phentolamine or unlabeled GTP. These findings provide direct evidence for the coupling of the alpha 1-adrenergic receptor to a previously uncharacterized G-protein (termed Gh), which has an apparent molecular mass of approximately 74 kDa.
采用两种不同方法鉴定了参与α1 - 肾上腺素能受体信号传导的G蛋白。首先,将纯化的大鼠肝细胞膜与[α - 32P]GTP在无或有肾上腺素能激动剂( - ) - 肾上腺素存在的情况下,或在有GTP存在的情况下孵育。经过紫外线照射、十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳和放射自显影后,许多蛋白质的共价标记明显可见,且可被未标记的GTP阻断。在仅用( - ) - 肾上腺素处理的制剂中,一种74 kDa蛋白的标记明显增强。还观察到40 - 50 kDa蛋白的标记增强。在由富含α1 - 肾上腺素能受体的FRTL - 5甲状腺细胞制备的类似处理的膜中,74 kDa蛋白的标记也很明显,但在由基本不含α1 - 受体的火鸡红细胞或NIH 3T3成纤维细胞制备的膜中则不明显。其次,通过将纯化的大鼠肝细胞膜与( - ) - 肾上腺素孵育来诱导α1 - 激动剂 - 受体 - G蛋白三元复合物的形成。加入利血平(浓度为10( - 7)M)和(±) - 普萘洛尔(浓度为10( - 6)M)以防止( - ) - 肾上腺素激活α2 - 和β - 肾上腺素能受体。将激素、受体和G蛋白的三元复合物溶解,用肝素和麦胚凝集素 - 琼脂糖进行部分纯化,然后重构成磷脂囊泡。这些囊泡显示出激动剂刺激的鸟苷5'-O - 3 - 硫代三磷酸(GTPγS)结合,该结合被酚妥拉明(浓度为10( - 4)M)阻断。相比之下,当囊泡与β - 激动剂异丙肾上腺素孵育时,GTPγS结合的刺激不明显。在( - ) - 肾上腺素存在的情况下,将囊泡与[α - 32P]GTP或[α - 32P]叠氮基 - GTP孵育,然后进行光解、十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳和放射自显影,导致一种74 kDa蛋白的共价标记。该蛋白的标记可通过用酚妥拉明或未标记的GTP预孵育来阻断。这些发现为α1 - 肾上腺素能受体与一种先前未鉴定的G蛋白(称为Gh)的偶联提供了直接证据;该G蛋白的表观分子量约为74 kDa。