Suppr超能文献

异丙肾上腺素和鸟苷亚氨基二磷酸共同作用于青蛙红细胞膜所产生的腺苷酸环化酶系统的持续激活状态。

A persistent active state of the adenylate cyclase system produced by the combined actions of isoproterenol and guanylyl imidodiphosphate in frog erythrocyte membranes.

作者信息

Schramm M, Rodbell M

出版信息

J Biol Chem. 1975 Mar 25;250(6):2232-7.

PMID:163823
Abstract

Isoproterenol plus guanylyl imidodiphosphate (Gpp(NH)p) activate frog erythrocyte adenylate cyclase to a level much higher than the sum of the activities produced by the catecholamine and the synthetic nucleotide tested separately. Propranolol, the beta-receptor blocking agent, failed to inhibit activity when added after the enzyme system had been preincubated with both isoproterenol and Gpp(NH)p. However, if propranolol was added after only one of the two components had been added, it inhibited the effect of isoproterenol. Production of the propranolol-resistant state by treatment with isoproterenol and Gpp(NH)p did not require the presence of the productive substrate (MgATP). The activated propranolol-resistant state persisted following various treatments of the enzyme preparation including extensive washings of the membranes; considerable activity was retained even after sonication or treatment with the detergent Lubrol-PX, treatments which caused inactivation of the native enzyme. Extensive dilution of the membranes following pretreatment with isoproterenol and Gpp(NH)p did not significantly reduce to the activity of the enzyme. Readdition of isoproterenol after dilution caused some inhibition of adenylate cyclase activity, indicating apparently that the beta-receptor has not become inaccessible. In contrast, preincubation with isoproterenol alone failed to render the enzyme system refractive to propranolol, and dilution readily reduced the activity to negligibly low values. Preincubation with Gpp(NH)p alone also produced a persistent active state but the activity was much lower than that obtained throught the combined action of isoproterenol and Gpp(NH)p. The findings suggest that the hormone may be required only to facilitate the initial interaction of the enzyme with Gpp(NH)p. The differences, in this respect, between Gpp(NH)p and the more labile natural nucleotide, GTP, are discussed.

摘要

异丙肾上腺素加鸟苷酰亚胺二磷酸(Gpp(NH)p)可将青蛙红细胞腺苷酸环化酶激活至比分别测试的儿茶酚胺和合成核苷酸所产生的活性总和高得多的水平。β受体阻滞剂普萘洛尔在酶系统与异丙肾上腺素和Gpp(NH)p预孵育后添加时,未能抑制活性。然而,如果仅在添加两种成分之一后添加普萘洛尔,则它会抑制异丙肾上腺素的作用。用异丙肾上腺素和Gpp(NH)p处理产生对普萘洛尔耐药的状态并不需要有活性的底物(MgATP)存在。在对酶制剂进行各种处理(包括对膜进行大量洗涤)后,对普萘洛尔耐药的激活状态仍然存在;即使在超声处理或用去污剂Lubrol-PX处理后,仍保留相当的活性,而这些处理会导致天然酶失活。用异丙肾上腺素和Gpp(NH)p预处理后对膜进行大量稀释并没有显著降低酶的活性。稀释后重新添加异丙肾上腺素会对腺苷酸环化酶活性产生一些抑制,这显然表明β受体并未变得无法接近。相比之下,仅用异丙肾上腺素预孵育未能使酶系统对普萘洛尔产生抗性,并且稀释很容易将活性降低到可忽略不计的低值。仅用Gpp(NH)p预孵育也产生了持续的活性状态,但活性远低于通过异丙肾上腺素和Gpp(NH)p共同作用所获得的活性。这些发现表明,可能仅需要激素来促进酶与Gpp(NH)p的初始相互作用。本文讨论了在这方面Gpp(NH)p与更不稳定的天然核苷酸GTP之间的差异。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验