Suppr超能文献

P2Y嘌呤能受体激动剂和鸟嘌呤核苷酸对磷脂酶C的激活动力学

Kinetics of activation of phospholipase C by P2Y purinergic receptor agonists and guanine nucleotides.

作者信息

Boyer J L, Downes C P, Harden T K

机构信息

Department of Pharmacology, University of North Carolina, School of Medicine, Chapel Hill 27599.

出版信息

J Biol Chem. 1989 Jan 15;264(2):884-90.

PMID:2910869
Abstract

Membranes prepared from [3H]inositol-labeled turkey erythrocytes express a phospholipase C that is markedly stimulated by stable analogs of GTP (Harden, T. K., Stephens, L., Hawkins, P. T., and Downes, C. P. (1987) J. Biol. Chem. 262, 9057-9061). We now report that P2-purinergic receptor-mediated regulation of the enzyme occurs in the membrane preparation. The order of potency of a series of ATP and ADP analogs for stimulation of inositol phosphate formation, i.e. 2-methylthioadenosine 5'-triphosphate (2MeSATP) greater than adenosine 5'-O-(2-thiodiphosphate) greater than adenosine 5'-O-(3-thiotriphosphate) greater than ATP greater than 5'-adenylyl imidodiphosphate approximately ADP greater than alpha, beta-methyleneadenosine 5'-triphosphate greater than beta, gamma-methyleneadenosine 5'-triphosphate, was consistent with that for the P2Y-purinergic receptor subtype. Agonist-stimulated effects were completely dependent on the presence of guanine nucleotide. Activation of phospholipase C by guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S) occurred with a considerable time lag. The rate of activation followed first order kinetics and was markedly increased by increasing concentrations of a P2Y receptor agonist; in contrast, the rate of activation at a fixed agonist concentration was independent of guanine nucleotide concentration. Addition of guanosine 5'-O-(2-thiodiphosphate) (GDP beta S) prior to addition of agonist and GTP, 5'-guanylyl imidodiphosphate (Gpp(NH)p), or GTP gamma S blocked in a concentration-dependent manner the stimulatory effect of guanine nucleotide. GDP beta S, added subsequent to preactivation of membranes with 2MeSATP and GTP gamma S or Gpp(NH)p had only small inhibitory effects on the rate of inositol phosphate production observed over the subsequent 10 min. In contrast, addition of GDP beta S to GTP-preactivated membranes resulted in a rapid return of enzyme activity to the basal state within 60 s. Taken together, the data are consistent with the idea that P2Y receptor activation increases the rate of exchange of GTP and GTP analogs for GDP on the relevant guanine nucleotide regulatory protein. Once the active enzymic species is formed, hydrolysis of guanine nucleotide reverts the enzyme to the inactive state.

摘要

用[3H]肌醇标记的火鸡红细胞制备的膜表达一种磷脂酶C,该酶受到GTP稳定类似物的显著刺激(哈登,T.K.,斯蒂芬斯,L.,霍金斯,P.T.,和唐斯,C.P.(1987年)《生物化学杂志》262,9057 - 9061)。我们现在报告,在膜制备物中发生了P2 - 嘌呤能受体介导的该酶的调节。一系列ATP和ADP类似物刺激肌醇磷酸形成的效力顺序,即2 - 甲硫基腺苷5'-三磷酸(2MeSATP)大于腺苷5'-O -(2 - 硫代二磷酸)大于腺苷5'-O -(3 - 硫代三磷酸)大于ATP大于5'-腺苷酰亚胺二磷酸约等于ADP大于α,β - 亚甲基腺苷5'-三磷酸大于β,γ - 亚甲基腺苷5'-三磷酸,与P2Y - 嘌呤能受体亚型的顺序一致。激动剂刺激的效应完全依赖于鸟嘌呤核苷酸的存在。鸟苷5'-O -(3 - 硫代三磷酸)(GTPγS)激活磷脂酶C有相当长的时间延迟。激活速率遵循一级动力学,并且通过增加P2Y受体激动剂的浓度而显著增加;相反,在固定激动剂浓度下的激活速率与鸟嘌呤核苷酸浓度无关。在加入激动剂和GTP、5'-鸟苷酰亚胺二磷酸(Gpp(NH)p)或GTPγS之前加入鸟苷5'-O -(2 - 硫代二磷酸)(GDPβS)以浓度依赖的方式阻断鸟嘌呤核苷酸的刺激作用。在用2MeSATP和GTPγS或Gpp(NH)p预激活膜之后加入GDPβS,在随后的10分钟内对观察到的肌醇磷酸产生速率只有很小的抑制作用。相反,向GTP预激活的膜中加入GDPβS导致酶活性在60秒内迅速恢复到基础状态。综上所述,这些数据与以下观点一致,即P2Y受体激活增加了相关鸟嘌呤核苷酸调节蛋白上GTP和GTP类似物与GDP交换的速率。一旦形成活性酶物种,鸟嘌呤核苷酸的水解会使酶恢复到无活性状态。

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