Suppr超能文献

视杆细胞外段的GTP结合蛋白。I. 每个亚基在GTP水解循环中的作用。

The GTP-binding protein of rod outer segments. I. Role of each subunit in the GTP hydrolytic cycle.

作者信息

Yamazaki A, Tatsumi M, Torney D C, Bitensky M W

出版信息

J Biol Chem. 1987 Jul 5;262(19):9316-23.

PMID:3036854
Abstract

The GTP-binding protein of Bufo marinus rod outer segments (ROS) is composed of 3 subunits: G alpha, 39,000; G beta, 36,000; and G gamma, approximately 6,500. A stepwise analysis of the GTP hydrolytic cycle (GTP binding, GTP hydrolysis, and GDP release) was facilitated by using purified subunits of the GTP-binding protein. When G alpha and G beta, gamma concentrations were held constant, the initial rate of guanosine-5'-O-(3-thiotriphosphate) (GTP gamma-s) binding to G alpha was dependent upon the amount of bleached rhodopsin present (as illuminated, urea-washed ROS disc membranes). When G alpha and the quantity of these membranes was held constant, the initial rate of GTP gamma-s binding to G alpha was markedly enhanced by increasing the amount of G beta, gamma. G beta preparations (free of G gamma) also stimulated the binding of GTP gamma-s to G alpha to the same extent as G beta, gamma preparations, suggesting that G gamma is not an essential component of the G beta, gamma-dependent stimulation of the rate of GTP gamma-s binding to G alpha. Nonlinear regression analysis revealed a single class of binding sites with an apparent stoichiometry of 1 mol of site/mol of G alpha under optimal binding conditions. Following GTP binding to G alpha, the GTP X G alpha complex dissociates from G beta, gamma which remains primarily bound to the ROS disc membranes. Moreover, while GTP remains in excess, the rates of GTP hydrolysis exhibited saturation in the presence of increasing amounts of G beta, gamma. Nonlinear regression analysis of these data argues against a direct role for G beta, gamma in the hydrolysis of GTP. Thus, both topologic and kinetic data support the concept that GTP hydrolysis is carried out by G alpha alone. After hydrolysis of GTP, the GDP X G alpha complex returned to the ROS disc membrane when G beta, gamma was present on the membrane surface, in the presence and absence of light. Without guanine nucleotides GDP release occurred in the presence of illuminated ROS disc membranes and G beta, gamma. Guanine nucleotides (GTP gamma-s approximately equal to GTP approximately equal to guanosine 5'-(beta, gamma-imido)triphosphate greater than GDP) could effectively displace GDP from G alpha under these conditions.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

海蟾蜍视杆外段(ROS)的GTP结合蛋白由3个亚基组成:Gα,39000;Gβ,36000;以及Gγ,约6500。通过使用GTP结合蛋白的纯化亚基,对GTP水解循环(GTP结合、GTP水解和GDP释放)进行了逐步分析。当Gα和Gβ、γ的浓度保持恒定时,鸟苷-5'-O-(3-硫代三磷酸)(GTPγ-s)与Gα结合的初始速率取决于存在的漂白视紫红质的量(如经光照、尿素洗涤的ROS盘膜)。当Gα和这些膜的量保持恒定时,通过增加Gβ、γ的量,GTPγ-s与Gα结合的初始速率显著提高。Gβ制剂(不含Gγ)刺激GTPγ-s与Gα结合的程度与Gβ、γ制剂相同,这表明Gγ不是Gβ、γ依赖性刺激GTPγ-s与Gα结合速率的必需成分。非线性回归分析显示,在最佳结合条件下,存在一类结合位点,其表观化学计量为每摩尔Gα1摩尔位点。GTP与Gα结合后,GTP·Gα复合物从Gβ、γ解离,而Gβ、γ主要仍与ROS盘膜结合。此外,当GTP过量时,在Gβ、γ量增加的情况下,GTP水解速率呈现饱和。对这些数据的非线性回归分析表明Gβ、γ在GTP水解中没有直接作用。因此,拓扑学和动力学数据均支持GTP水解仅由Gα进行的概念。GTP水解后,当膜表面存在Gβ、γ时,无论有无光照,GDP·Gα复合物都会回到ROS盘膜。在有光照的ROS盘膜和Gβ、γ存在的情况下,没有鸟嘌呤核苷酸时会发生GDP释放。在这些条件下,鸟嘌呤核苷酸(GTPγ-s≈GTP≈鸟苷5'-(β,γ-亚氨基)三磷酸>GDP)可以有效地从Gα上取代GDP。(摘要截于400字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验