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Oxidative protein labeling with analysis by mass spectrometry for the study of structure, folding, and dynamics

机译:通过质谱分析对氧化蛋白进行标记,以研究结构,折叠和动力学

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Significance: Analytical approaches that can provide insights into the mechanistic processes underlying protein folding and dynamics are few since the target analytes - high-energy structural intermediates - are short lived and often difficult to distinguish from coexisting structures. Folding "intermediates" can be populated at equilibrium using weakly denaturing solvents, but it is not clear that these species are identical to those that are transiently populated during folding under "native" conditions. Oxidative labeling with mass spectrometric analysis is a powerful alternative for structural characterization of proteins and transient protein species based on solvent exposure at specific sites. Recent Advances: Oxidative labeling is increasingly used with exceedingly short (μs) labeling pulses, both to minimize the occurrence of artifactual structural changes due to the incorporation of label and to detect short-lived species. The recent introduction of facile photolytic approaches for producing reactive oxygen species is an important technological advance that will enable more widespread adoption of the technique. Critical Issues: The most common critique of oxidative labeling data is that even with brief labeling pulses, covalent modification of the protein may cause significant artifactual structural changes. Future Directions: While the oxidative labeling with the analysis by mass spectrometry is mature enough that most basic methodological issues have been addressed, a complete systematic understanding of side chain reactivity in the context of intact proteins is an avenue for future work. Specifically, there remain issues around the impact of primary sequence and side chain interactions on the reactivity of "solvent-exposed" residues. Due to its analytical power, wide range of applications, and relative ease of implementation, oxidative labeling is an increasingly important technique in the bioanalytical toolbox. Antioxid. Redox Signal. 21, 497-510.
机译:启示:由于目标分析物-高能结构中间体-寿命短并且通常难以与共存结构区分开,因此能够提供深入了解蛋白质折叠和动力学机理的分析方法很少。可以使用弱变性溶剂在平衡状态下填充折叠的“中间体”,但尚不清楚这些物质是否与“天然”条件下折叠过程中瞬时填充的物质相同。质谱分析的氧化标记是基于特定位置的溶剂暴露对蛋白质和瞬时蛋白质种类进行结构表征的有力替代方法。最新进展:氧化标记越来越多地用于超短(μs)标记脉冲,既可以最大程度地减少由于掺入标记而导致的人为结构变化的发生,也可以检测短命物种。最近引入的用于生产活性氧的简便光解方法是一项重要的技术进步,它将使该技术得到更广泛的采用。关键问题:对氧化标记数据的最普遍的批评是,即使短暂的标记脉冲,蛋白质的共价修饰也可能导致明显的人为结构变化。未来方向:尽管通过质谱分析进行的氧化标记已经足够成熟,可以解决大多数基本的方法学问题,但是完整系统地了解完整蛋白质范围内的侧链反应性仍是未来工作的途径。具体地,在一级序列和侧链相互作用对“溶剂暴露的”残基的反应性的影响方面仍然存在问题。由于其强大的分析能力,广泛的应用范围和相对容易实现的作用,因此氧化标记在生物分析工具箱中已成为越来越重要的技术。抗氧化。氧化还原信号。 21,497-510。

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