Ravindra R, Aronstam R S
Department of Medicine, East Carolina University, Greenville 27858-4354.
J Reprod Fertil. 1992 Aug;95(3):669-77. doi: 10.1530/jrf.0.0950669.
Plasma membranes (1-2 mg protein) purified from the anterior pituitary lobes of adult male rats were incubated with 0.6 mumol [alpha-32P]guanosine 5'-triphosphate (GTP) l-1 in an ATP-regenerating buffer at 37 degrees C for 60 min; during this incubation the [32P]GTP was hydrolysed and the nucleotide that was predominantly bound to the membranes was [32P]GDP. The release of [32P]GDP from the membranes was monitored at 37 degrees C; the amount released was proportional to the protein concentration and increased as a function of time. 5'-Guanylylimidodiphosphate (Gpp(NH)p) increased [32P]GDP release by up to 30% at 0.1 mumol l-1. Although 10 nmol Gpp(NH)p l-1 had no effect on GDP release, it appeared to stabilize the hormonal effect by blocking further GDP-GTP exchange. Gonadotrophin-releasing hormone (GnRH) agonist and thyrotrophin-releasing hormone (TRH), at 0.1 mumol l-1 caused a maximum increase in the release of [32P]GDP of 31-38%. The GnRH agonist (0.1 mumol l-1) stimulated GDP release by 21%, 24%, 17% and 14% at 30 s, 1, 2 and 5 min, respectively. TRH (0.1 mumol l-1) stimulated GDP release by 38%, 30%, 17% and 16% at 30 s, 1, 2 and 5 min, respectively. A GnRH antagonist also stimulated [32P]GDP release, albeit less effectively than GnRH agonist; the antagonist did not inhibit agonist stimulation of GDP release. These results indicate that ligand binding to the GnRH and TRH receptors results in interaction of the receptor with a guanine-nucleotide-dependent transducer protein (G protein) and activation of GTP-GDP exchange.(ABSTRACT TRUNCATED AT 250 WORDS)
从成年雄性大鼠垂体前叶纯化的质膜(1 - 2毫克蛋白质),在37℃的ATP再生缓冲液中与0.6微摩尔[α-32P]鸟苷5'-三磷酸(GTP)孵育60分钟;在此孵育过程中,[32P]GTP被水解,主要与膜结合的核苷酸是[32P]GDP。在37℃监测[32P]GDP从膜上的释放;释放量与蛋白质浓度成正比,并随时间增加。5'-鸟苷酰亚胺二磷酸(Gpp(NH)p)在0.1微摩尔/升时使[32P]GDP释放增加高达30%。尽管10纳摩尔/升的Gpp(NH)p对GDP释放没有影响,但它似乎通过阻断进一步的GDP - GTP交换来稳定激素效应。促性腺激素释放激素(GnRH)激动剂和促甲状腺激素释放激素(TRH),在0.1微摩尔/升时使[32P]GDP释放最多增加31 - 38%。GnRH激动剂(0.1微摩尔/升)在30秒、1、2和5分钟时分别刺激GDP释放21%、24%、17%和14%。TRH(0.1微摩尔/升)在30秒、1、2和5分钟时分别刺激GDP释放38%、30%、17%和16%。一种GnRH拮抗剂也刺激[32P]GDP释放,尽管效果不如GnRH激动剂;该拮抗剂不抑制激动剂对GDP释放的刺激。这些结果表明,配体与GnRH和TRH受体结合导致受体与鸟嘌呤核苷酸依赖性转导蛋白(G蛋白)相互作用并激活GTP - GDP交换。(摘要截断于250字)