Suppr超能文献

六聚体大肠杆菌精氨酸阻遏物的对称变构机制利用了 L-精氨酸配体和固有精氨酸残基之间的竞争。

Symmetric allosteric mechanism of hexameric Escherichia coli arginine repressor exploits competition between L-arginine ligands and resident arginine residues.

机构信息

Chemistry Department, Princeton University, Princeton, New Jersey, USA.

出版信息

PLoS Comput Biol. 2010 Jun 3;6(6):e1000801. doi: 10.1371/journal.pcbi.1000801.

Abstract

An elegantly simple and probably ancient molecular mechanism of allostery is described for the Escherichia coli arginine repressor ArgR, the master feedback regulator of transcription in L-arginine metabolism. Molecular dynamics simulations with ArgRC, the hexameric domain that binds L-arginine with negative cooperativity, reveal that conserved arginine and aspartate residues in each ligand-binding pocket promote rotational oscillation of apoArgRC trimers by engagement and release of hydrogen-bonded salt bridges. Binding of exogenous L-arginine displaces resident arginine residues and arrests oscillation, shifting the equilibrium quaternary ensemble and promoting motions that maintain the configurational entropy of the system. A single L-arg ligand is necessary and sufficient to arrest oscillation, and enables formation of a cooperative hydrogen-bond network at the subunit interface. The results are used to construct a free-energy reaction coordinate that accounts for the negative cooperativity and distinctive thermodynamic signature of L-arginine binding detected by calorimetry. The symmetry of the hexamer is maintained as each ligand binds, despite the conceptual asymmetry of partially-liganded states. The results thus offer the first opportunity to describe in structural and thermodynamic terms the symmetric relaxed state predicted by the concerted allostery model of Monod, Wyman, and Changeux, revealing that this state is achieved by exploiting the dynamics of the assembly and the distributed nature of its cohesive free energy. The ArgR example reveals that symmetry can be maintained even when binding sites fill sequentially due to negative cooperativity, which was not anticipated by the Monod, Wyman, and Changeux model. The molecular mechanism identified here neither specifies nor requires a pathway for transmission of the allosteric signal through the protein, and it suggests the possibility that binding of free amino acids was an early innovation in the evolution of allostery.

摘要

一种优雅简单且可能古老的变构作用分子机制被描述为大肠杆菌精氨酸阻遏物 ArgR,这是 L-精氨酸代谢中转录的主反馈调节剂。ArgRC 的分子动力学模拟,即与 L-精氨酸具有负协同性结合的六聚体结构域,揭示了每个配体结合口袋中保守的精氨酸和天冬氨酸残基通过氢键盐桥的结合和释放促进apoArgRC 三聚体的旋转振荡。外源性 L-精氨酸的结合取代了固有精氨酸残基并阻止了振荡,从而改变了平衡的四级聚集体并促进了维持系统构象熵的运动。单个 L-精氨酸配体是必需且足够的,以阻止振荡,并能够在亚基界面形成协同氢键网络。结果用于构建自由能反应坐标,以解释由量热法检测到的 L-精氨酸结合的负协同性和独特热力学特征。尽管部分配体状态具有概念上的不对称性,但六聚体的对称性仍得以维持,因为每个配体结合。因此,结果首次有机会以结构和热力学术语描述 Monod、Wyman 和 Changeux 的协同变构模型预测的对称松弛状态,揭示了该状态是通过利用组装的动力学和其内聚自由能的分布式性质来实现的。ArgR 的例子表明,即使由于负协同性导致结合位点依次填充,对称性也可以保持,这是 Monod、Wyman 和 Changeux 模型所没有预料到的。这里确定的分子机制既没有指定也不需要变构信号通过蛋白质传递的途径,并且它表明自由氨基酸结合可能是变构作用进化的早期创新。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e32b/2880562/03601c7aee60/pcbi.1000801.g001.jpg

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