Feder D, Im M J, Pfeuffer T, Hekman M, Helmreich E J, Levitzki A
Biochem Soc Symp. 1986;52:145-51.
The regulation of adenylate cyclase by hormones and by GTP regulatory proteins was investigated in native membrane systems and in systems reconstituted from purified components. These studies can be summarized as follows. The stimulatory beta 1-adrenoceptor catalyses the activation of a complex between the GTP stimulatory protein GS and the catalytic unit C. The agonist-receptor complex can activate a few cyclase units in native membrane systems as well as in reconstituted systems. GS from turkey erythrocytes is functionally different from rabbit liver GS, the latter being more amenable to activation by guanyl nucleotides in the absence of hormone. The coupling between the beta 1-adrenoceptor GS and C is efficient when compared with the coupling obtained in native membrane systems. GTP/GDP exchange at the alpha S subunit requires the presence of the beta gamma subunits. A mechanism for the inhibition of adenylate cyclase by the inhibitory GTP regulatory protein Gi is suggested.
在天然膜系统和由纯化成分重构的系统中,研究了激素和GTP调节蛋白对腺苷酸环化酶的调节作用。这些研究可总结如下。刺激性β1 -肾上腺素能受体催化GTP刺激性蛋白GS与催化单位C之间复合物的激活。激动剂 - 受体复合物可激活天然膜系统以及重构系统中的一些环化酶单位。来自火鸡红细胞的GS在功能上与兔肝GS不同,后者在无激素的情况下更易于被鸟苷核苷酸激活。与天然膜系统中获得的偶联相比,β1 -肾上腺素能受体GS与C之间的偶联效率更高。αS亚基上的GTP / GDP交换需要βγ亚基的存在。提出了抑制性GTP调节蛋白Gi抑制腺苷酸环化酶的机制。