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Mass Spectrometry-Based Protein Footprinting for Higher-Order Structure Analysis: Fundamentals and Applications

机译:基于质谱的蛋白质足迹,用于高阶结构分析:基础和应用

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Proteins adopt different higher-order structures (HOS) to enable their unique biological functions. Understanding the complexities of protein higher-order structures and dynamics requires integrated approaches, where mass spectrometry (MS) is now positioned to play a key role. One of those approaches is protein footprinting. Although the initial demonstration of footprinting was for the HOS determination of protein/nucleic acid binding, the concept was later adapted to MS-based protein HOS analysis, through which different covalent labeling approaches "mark" the solvent accessible surface area (SASA) of proteins to reflect protein HOS. Hydrogen-deuterium exchange (HDX), where deuterium in D2O replaces hydrogen of the backbone amides, is the most common example of footprinting. Its advantage is that the footprint reflects SASA and hydrogen bonding, whereas one drawback is the labeling is reversible. Another example of footprinting is slow irreversible labeling of functional groups on amino acid side chains by targeted reagents with high specificity, probing structural changes at selected sites. A third footprinting approach is by reactions with fast, irreversible labeling species that are highly reactive and footprint broadly several amino acid residue side chains on the time scale of submilliseconds. All of these covalent labeling approaches combine to constitute a problem-solving toolbox that enables mass spectrometry as a valuable tool for HOS elucidation. As there has been a growing need for MS-based protein footprinting in both academia and industry owing to its high throughput capability, prompt availability, and high spatial resolution, we present a summary of the history, descriptions, principles, mechanisms, and applications of these covalent labeling approaches. Moreover, their applications are highlighted according to the biological questions they can answer. This review is intended as a tutorial for MS-based protein HOS elucidation and as a reference for investigators seeking a MS-based tool to address structural questions in protein science.
机译:蛋白质采用不同的高阶结构(HOS)来实现其独特的生物功能。了解蛋白质高阶结构和动力学的复杂性需要综合方法,其中质谱(MS)现在定位以发挥关键作用。其中一个方法是蛋白质足迹。虽然足迹的初始证明是术语的术语确定蛋白质/核酸结合,但该概念后来适用于MS的蛋白质HOS分析,通过该蛋白质hos分析,不同的共价标记方法“标记”蛋白质的溶剂可接近的表面积(SASA)。蛋白质反射蛋白质hos。氢 - 氘交换(HDX),D2O氘代替骨干酰胺的氢,是脚印的最常见的例子。其优点是占地面积反映了SASA和氢键,而一个缺点是标签是可逆的。通过具有高特异性的靶向试剂,氨基酸侧链上的官能团的官能团的另一个例子是慢性不可逆标记,探测所选地点的结构变化。第三种脚印方法是用快速,不可逆的标记物种的反应,其具有高反应性和占地面积,在亚硫腙的时间等级上广泛几个氨基酸残基侧链。所有这些共价标记方法都结合起来构成了解决问题的工具箱,使得质谱是作为HOS阐明的有价值的工具。由于由于其高吞吐量能力,提示可用性和高空间解决方案,因此在学术界和工业中越来越需要在学术界和工业中,我们概述了历史,描述,原则,机制和应用的摘要这些共价标记方法。此外,他们的应用程序根据他们可以回答的生物学问题突出显示。本综述旨在作为MS的蛋白质母语阐释的教程,并作为寻求基于MS的工具的调查人员来解决蛋白质科学的结构问题的参考。

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