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通过压力弛豫研究确定的延伸因子Ts促进延伸因子Tu释放核苷酸的动力学机制。

The kinetic mechanism of the release of nucleotide from elongation factor Tu promoted by elongation factor Ts determined by pressure relaxation studies.

作者信息

Eccleston J F, Kanagasabai T F, Geeves M A

机构信息

National Institute for Medical Research, Mill Hill, London, United Kingdom.

出版信息

J Biol Chem. 1988 Apr 5;263(10):4668-72.

PMID:3350808
Abstract

The release of a chromophoric analogue of GDP, 2-amino-6-mercaptopurine riboside 5'-diphosphate (thioGDP), from its complex with elongation factor Tu (EF-Tu) is catalyzed by elongation factor Ts (EF-Ts). The mechanism of this reaction includes a ternary complex; EF-Tu.thioGDP.EF-Ts (Eccleston, J. F. (1984) J. Biol. Chem. 259, 12997-13003). This mechanism has been further investigated using pressure relaxation techniques combined with spectrophotometric measurements. The equilibrium of a solution of EF-Tu, EF-Ts, and thioGDP over a range of concentrations is perturbed on increasing the pressure to 150 atm. Rapid decrease of the pressure back to 1 atm results in a biphasic relaxation process, an initial fast phase which is complete within 1 ms followed by a slower phase. This is interpreted as the result of an isomerization of the EF-Tu.thioGDP.EF-Ts ternary complex which occurs before the release of thioGDP. Such an isomerization process may be a general feature in the release of GDP from guanosine nucleotide-binding proteins.

摘要

GDP的发色类似物2-氨基-6-巯基嘌呤核糖核苷5'-二磷酸(硫代GDP)从其与延伸因子Tu(EF-Tu)的复合物中的释放由延伸因子Ts(EF-Ts)催化。该反应机制包括一个三元复合物;EF-Tu·硫代GDP·EF-Ts(埃克莱斯顿,J.F.(1984年)《生物化学杂志》259卷,12997 - 13003页)。已使用压力弛豫技术结合分光光度测量对该机制进行了进一步研究。在将压力增加到150个大气压时,EF-Tu、EF-Ts和硫代GDP溶液在一系列浓度范围内的平衡受到扰动。将压力迅速降至1个大气压会导致双相弛豫过程,初始的快速相在1毫秒内完成,随后是较慢的相。这被解释为硫代GDP释放之前EF-Tu·硫代GDP·EF-Ts三元复合物异构化的结果。这种异构化过程可能是鸟苷核苷酸结合蛋白释放GDP的一个普遍特征。

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