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核苷二磷酸激酶在GTP结合蛋白上将GDP转化为GTP。

Conversion of GDP into GTP by nucleoside diphosphate kinase on the GTP-binding proteins.

作者信息

Kikkawa S, Takahashi K, Takahashi K, Shimada N, Ui M, Kimura N, Katada T

机构信息

Department of Life Science, Tokyo Institute of Technology, Yohohama, Japan.

出版信息

J Biol Chem. 1990 Dec 15;265(35):21536-40.

PMID:2174878
Abstract

A direct interaction of alpha beta gamma trimeric GTP binding proteins (G proteins; G0 and Gs) with nucleoside diphosphate kinase (NDP kinase) was investigated with homogeneously purified proteins. There was a progressive release of 32Pi from [gamma-32P]ATP when GDP-bound G0 was incubated together with NDP kinase. The Pi release induced by the interaction of G0 with NDP kinase was not accompanied by the dissociation of GDP bound to the alpha-subunit of G0. This was a sharp contrast to G protein-catalyzed GTP hydrolysis observed with GTP as the substrate; the dissociation of bound GDP was essentially required for the following binding of the substrate, GTP, to be hydrolyzed. A kinetic analysis displayed different properties for the substrate of NDP kinase between free GDP and G protein-bound GDP. NDP kinase-dependent phosphorylation of GDP on G0 was indeed demonstrated with adenosine 5'-(3-O-thio)triphosphate as the phosphate donor; there was a formation of guanosine 5'-(3-O-thio)triphosphate-bound G0 from the ATP analogue. Moreover, purified Gs was readily ADP-ribosylated by cholera toxin in the presence of NDP kinase, ATP, and an ADP-ribosylation factor, also suggesting that the nucleotide form on Gs was certainly GTP. These results indicate that NDP kinase can transfer the gamma-phosphate of ATP directly to GDP bound to G proteins and that this phosphorylation results in the activation of the signal-coupling proteins. A possible role of the new activation mechanism of G proteins is discussed in comparison with the previously characterized GDP-GTP exchange pathway by the agonist-receptor complex.

摘要

利用均一纯化的蛋白质研究了αβγ三聚体GTP结合蛋白(G蛋白;G0和Gs)与核苷二磷酸激酶(NDP激酶)之间的直接相互作用。当将结合GDP的G0与NDP激酶一起孵育时,[γ-32P]ATP中的32Pi会逐渐释放。G0与NDP激酶相互作用诱导的Pi释放并未伴随着与G0α亚基结合的GDP的解离。这与以GTP为底物观察到的G蛋白催化的GTP水解形成了鲜明对比;底物GTP随后的结合水解基本上需要结合的GDP解离。动力学分析显示,游离GDP和G蛋白结合的GDP作为NDP激酶底物具有不同的特性。以腺苷5'-(3-O-硫代)三磷酸作为磷酸供体,确实证明了NDP激酶对G0上的GDP进行依赖性磷酸化;由ATP类似物形成了结合鸟苷5'-(3-O-硫代)三磷酸的G0。此外,在NDP激酶、ATP和ADP-核糖基化因子存在的情况下,纯化的Gs很容易被霍乱毒素进行ADP-核糖基化,这也表明Gs上的核苷酸形式肯定是GTP。这些结果表明,NDP激酶可以将ATP的γ-磷酸基团直接转移到与G蛋白结合的GDP上,并且这种磷酸化导致信号偶联蛋白的激活。与先前由激动剂-受体复合物表征的GDP-GTP交换途径相比,讨论了G蛋白新激活机制的可能作用。

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