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首页> 外文期刊>Biochemistry >Monitoring aromatic picosecond to nanosecond dynamics in proteins via C-13 relaxation: Expanding perturbation mapping of the rigidifying core mutation, V54A, in Eglin C
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Monitoring aromatic picosecond to nanosecond dynamics in proteins via C-13 relaxation: Expanding perturbation mapping of the rigidifying core mutation, V54A, in Eglin C

机译:通过C-13弛豫监测蛋白质中的皮秒级至纳秒级动力学:扩大Eglin C中刚性核突变V54A的扰动图谱

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摘要

Long-range effects, such as allostery, have evolved in proteins as a means of regulating function via communication between distal sites. An NMR-based perturbation mapping approach was used to more completely probe the dynamic response of the core mutation V54A in the protein eglin c by monitoring changes in picosecond to nanosecond aromatic side-chain dynamics and H/D exchange stabilities. Previous side-chain dynamics studies on this mutant were limited to methyl-bearing residues, most of which were found to rigidify on the picosecond to nanosecond time scale in the form of a contiguous "network". Here, high precision C-13 relaxation data from 13 aromatic side chains were acquired by applying canonical relaxation experiments to a newly developed carbon labeling scheme [Teilum et al. (2006) J. Am. Chem. Soc. 128, 2506-2507]. The fitting of model-free parameters yielded S-2 variability which is intermediate with respect to backbone and methyl-bearing side-chain variability and tau(e) values that are approximately Ins. Inclusion of the aromatic dynamic response results in an expanded network of dynamically coupled residues, with some aromatics showing increases in flexibility, which partially offsets the rigidification in methyl side chains. Using amide hydrogen exchange, dynamic propagation on a slower time scale was probed in response to the V54A perturbation. Surprisingly, regional stabilization (slowed exchange) 10-12 angstrom from the site of mutation was observed despite a global destabilization of 1.5 kcal.mol(-1). Furthermore, this unlikely pocket of stabilized residues colocalizes with increases in aromatic flexibility on the faster time scale. Because the converse is also true (destabilized residues colocalize with rigidification on the fast time scale), a plausible entropy-driven mechanism is discussed for relating colocalization of opposing dynamic trends on vastly different time scales.
机译:诸如变构等远距离效应已在蛋白质中发展,作为通过远端位点之间的交流调节功能的手段。通过监测从皮秒到纳秒级的芳香族侧链动力学和H / D交换稳定性的变化,基于NMR的扰动映射方法用于更完整地探测蛋白质eglin c中核心突变V54A的动态响应。先前对该突变体进行的侧链动力学研究仅限于含甲基的残基,发现大多数残基在皮秒至纳秒的时间尺度上以连续的“网络”形式僵化。在这里,通过将规范弛豫实验应用于新开发的碳标记方案,获得了来自13个芳族侧链的高精度C-13弛豫数据[Teilum等。 (2006)J. Am。化学Soc。 128,2506-2507]。无模型参数的拟合产生了S-2变异性,该变异性相对于骨架和含甲基的侧链变异性和tau(e)值大约为Ins。包含芳香族动态响应会导致动态耦合残基的扩展网络,某些芳香族化合物显示出柔性的增加,从而部分抵消了甲基侧链的刚性。使用酰胺氢交换,响应V54A扰动,在较慢的时间尺度上进行了动态传播。出乎意料的是,尽管全局失稳1.5 kcal.mol(-1),但仍观察到从突变位点起10-12埃的区域稳定(交换缓慢)。此外,这种不太可能的稳定残留物与芳香族柔韧性的增加在更快的时间范围内共定位。因为相反的情况也是正确的(不稳定的残基在快速的时间尺度上与刚性共定位),所以讨论了一种可能的熵驱动机制,用于将截然不同的时间尺度上相反的动态趋势的共定位相关联。

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