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放射性标记激动剂与磷脂酶C偶联的P2y嘌呤能受体的鸟嘌呤核苷酸敏感性相互作用。

Guanine nucleotide-sensitive interaction of a radiolabeled agonist with a phospholipase C-linked P2y-purinergic receptor.

作者信息

Cooper C L, Morris A J, 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 Apr 15;264(11):6202-6.

PMID:2495280
Abstract

Analogs of ATP and ADP produce a guanine nucleotide-dependent activation of phospholipase C in turkey erythrocyte membranes with pharmacological properties consistent with those of a P2y-purinergic receptor (Boyer, J. L., Downes, C. P., and Harden, T.K. (1989) J. Biol. Chem. 264, 884-890). This study describes the interaction of adenosine-5'-O-2-thio[35S] diphosphate ([35S]ADP beta S) with this putative P2y-purinergic receptor on purified plasma membranes prepared from turkey erythrocytes. In binding assays performed at 30 degrees C, the association rate constant of [35S] was 1.1 x 10(7) M-1 min-1 and the dissociation rate constant was 3.8 x 10(-2) min-1. [35S]ADP beta S bound with high affinity (Kd = 6-10 nM) to an apparently homogeneous population of sites (Bmax = 2-4 pmol/mg protein). ATP and ADP analogs (2-methylthio ATP, ADP beta S, ATP, ADP, 5'-adenylyl imidodiphosphate, alpha, beta-methylene adenosine-5'-triphosphate, and beta, gamma-methylene adenosine 5'-triphosphate) inhibited the binding of [35S]ADP beta S with properties consistent with ligand interaction by simple law of mass action kinetics at a single site. The rank order of potency for inhibition of [35S]ADP beta S binding was identical to the potency order observed for these same agonists for stimulation of phospholipase C in turkey erythrocyte ghosts. Guanine nucleotides inhibited [35S]ADP beta S binding in a noncompetitive manner with the following potency order: guanosine 5'-O-(3-thiotriphosphate) greater than 5'-guanylyl imidodiphosphate greater than GTP = GDP greater than guanosine 5'-O-2-(thiodiphosphate). The data are consistent with the idea that [35S]ADP beta S may be used to radiolabel the P2y-purinergic receptor linked to activation of phospholipase C in turkey erythrocyte membranes. In addition, interaction of radiolabeled agonist with the receptor is modified by guanine nucleotides, providing evidence that an agonist-induced receptor/guanine nucleotide regulatory protein complex may be involved in P2y-receptor action.

摘要

ATP和ADP的类似物可使火鸡红细胞膜中的磷脂酶C发生鸟嘌呤核苷酸依赖性激活,其药理学特性与P2y嘌呤能受体一致(博耶尔,J.L.,唐斯,C.P.,和哈登,T.K.(1989年)《生物化学杂志》264,884 - 890)。本研究描述了腺苷 - 5'-O - 2 - 硫代[35S]二磷酸([35S]ADPβS)与从火鸡红细胞制备的纯化质膜上这种假定的P2y嘌呤能受体的相互作用。在30℃进行的结合试验中,[35S]的缔合速率常数为1.1×10(7) M-1 min-1,解离速率常数为3.8×10(-2) min-1。[35S]ADPβS以高亲和力(Kd = 6 - 10 nM)结合到一个明显均一的位点群体(Bmax = 2 - 4 pmol/mg蛋白质)。ATP和ADP类似物(2 - 甲硫基ATP、ADPβS、ATP、ADP、5'-腺苷酰亚胺二磷酸、α,β - 亚甲基腺苷 - 5'-三磷酸和β,γ - 亚甲基腺苷5'-三磷酸)抑制[35S]ADPβS的结合,其特性符合单一位点上简单质量作用动力学的配体相互作用。抑制[35S]ADPβS结合的效力顺序与这些相同激动剂在火鸡红细胞血影中刺激磷脂酶C所观察到的效力顺序相同。鸟嘌呤核苷酸以非竞争性方式抑制[35S]ADPβS结合,效力顺序如下:鸟苷5'-O - (3 - 硫代三磷酸)>5'-鸟苷酰亚胺二磷酸>GTP = GDP>鸟苷5'-O - 2 - (硫代二磷酸)。这些数据与以下观点一致,即[35S]ADPβS可用于对与火鸡红细胞膜中磷脂酶C激活相关的P2y嘌呤能受体进行放射性标记。此外,放射性标记激动剂与受体的相互作用受到鸟嘌呤核苷酸的修饰,这提供了证据表明激动剂诱导的受体/鸟嘌呤核苷酸调节蛋白复合物可能参与P2y受体作用。

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