Londos C, Salomon Y, Lin M C, Harwood J P, Schramm M, Wolff J, Rodbell M
Proc Natl Acad Sci U S A. 1974 Aug;71(8):3087-90. doi: 10.1073/pnas.71.8.3087.
5'-Guanylylimidodiphosphate (Gpp(NH)-p) stimulates adenylate cyclase [ATP-pyrophosphate-lyase (cyclizing), EC 4.6.1.1] activity in plasma membranes isolated from frog and salmon erythrocytes, from rat adrenal, hepatic, and fat cells, and from bovine thyroid cells. The nucleotide acts cooperatively with the various hormones (glucagon, secretin, ACTH, thyrotropin, and catecholamines) that stimulate these adenylate cyclase systems with resultant activities that equal or exceed those obtained with hormone plus GTP or with fluoride ion. In the absence of hormones, Gpp(NH)p is a considerably more effective activator than GTP, and, under certain conditions of incubation, stimulates rat fat cell adenylate cyclase to levels of activity (about 20 nmoles of 3',5'-adenosine monophosphate mg protein per min) far higher than reported hitherto for any adenylate cyclase system examined. The nucleotide activates frog erythrocyte adenylate cyclase when the catecholamine receptor is blocked by the competitive antagonist, propranolol, and activates the enzyme from an adrenal tumor cell line which lacks functional ACTH receptors. In contrast, Gpp(NH)p does not stimulate adenylate cyclase in extracts from Escherichia coli B. Gpp(NH)p appears to be a useful probe for investigating the mechanism of hormone and nucleotide action on adenylate cyclase systems in eukaryotic cells.
5'-鸟苷酰亚胺二磷酸(Gpp(NH)-p)可刺激从青蛙和鲑鱼红细胞、大鼠肾上腺细胞、肝细胞、脂肪细胞以及牛甲状腺细胞中分离出的质膜中的腺苷酸环化酶[ATP-焦磷酸裂解酶(环化),EC 4.6.1.1]活性。该核苷酸与各种激素(胰高血糖素、促胰液素、促肾上腺皮质激素、促甲状腺激素和儿茶酚胺)协同作用,这些激素刺激这些腺苷酸环化酶系统,其产生的活性等于或超过激素加GTP或氟离子所获得的活性。在没有激素的情况下,Gpp(NH)p是比GTP更有效的激活剂,并且在某些孵育条件下,可将大鼠脂肪细胞腺苷酸环化酶的活性刺激到(每分钟约20纳米摩尔3',5'-腺苷单磷酸/毫克蛋白质)远远高于迄今为止所检测的任何腺苷酸环化酶系统所报道的水平。当儿茶酚胺受体被竞争性拮抗剂普萘洛尔阻断时,该核苷酸可激活青蛙红细胞腺苷酸环化酶,并可激活来自缺乏功能性促肾上腺皮质激素受体的肾上腺肿瘤细胞系的该酶。相比之下,Gpp(NH)p不会刺激大肠杆菌B提取物中的腺苷酸环化酶。Gpp(NH)p似乎是研究激素和核苷酸对真核细胞中腺苷酸环化酶系统作用机制的有用探针。