Living Systems Institute, Department of Biosciences, University of Exeter, Stocker Road, Exeter, EX4 4QD, U.K.
CPI, Darlington DL1 1GL, U.K.
Anal Chem. 2023 Mar 21;95(11):5000-5008. doi: 10.1021/acs.analchem.2c05310. Epub 2023 Mar 9.
Amide hydrogen/deuterium-exchange mass spectrometry (HDX-MS) is a powerful tool for analyzing the conformational dynamics of proteins in a solution. Current conventional methods have a measurement limit starting from several seconds and are solely reliant on the speed of manual pipetting or a liquid handling robot. Weakly protected regions of polypeptides, such as in short peptides, exposed loops and intrinsically disordered the protein exchange on the millisecond timescale. Typical HDX methods often cannot resolve the structural dynamics and stability in these cases. Numerous academic laboratories have demonstrated the considerable utility of acquiring HDX-MS data in the sub-second regimes. Here, we describe the development of a fully automated HDX-MS apparatus to resolve amide exchange on the millisecond timescale. Like conventional systems, this instrument boasts automated sample injection with software selection of labeling times, online flow mixing and quenching, while being fully integrated with a liquid chromatography-MS system for existing standard "bottom-up" workflows. HDX-MS's rapid exchange kinetics of several peptides demonstrate the repeatability, reproducibility, back-exchange, and mixing kinetics achieved with the system. Comparably, peptide coverage of 96.4% with 273 peptides was achieved, supporting the equivalence of the system to standard robotics. Additionally, time windows of 50 ms-300 s allowed full kinetic transitions to be observed for many amide groups; especially important are short time points (50-150 ms) for regions that are likely highly dynamic and solvent- exposed. We demonstrate that information on structural dynamics and stability can be measured for stretches of weakly stable polypeptides in small peptides and in local regions of a large enzyme, glycogen phosphorylase.
酰胺氢/氘交换质谱(HDX-MS)是分析溶液中蛋白质构象动力学的有力工具。目前的常规方法的测量起始时间从几秒开始,并且完全依赖于手动移液或液体处理机器人的速度。多肽的弱保护区域,如短肽、暴露环和固有无序蛋白,在毫秒时间尺度上交换。典型的 HDX 方法通常无法在这些情况下解析结构动力学和稳定性。许多学术实验室已经证明,在亚秒级范围内获取 HDX-MS 数据具有很大的实用性。在这里,我们描述了一种全自动 HDX-MS 仪器的开发,以在毫秒时间尺度上解析酰胺交换。与传统系统一样,该仪器具有自动进样功能,并具有软件选择标记时间、在线流动混合和淬火功能,同时与液相色谱-MS 系统完全集成,用于现有的标准“自上而下”工作流程。几种肽的 HDX-MS 快速交换动力学证明了该系统实现的重复性、再现性、反向交换和混合动力学。相比之下,用 273 个肽实现了 96.4%的肽覆盖率,支持该系统与标准机器人的等效性。此外,50 ms-300 s 的时间窗口允许对许多酰胺基团进行完整的动力学转变观察;对于可能高度动态和溶剂暴露的区域,短时间点(50-150 ms)尤其重要。我们证明,对于小肽中的弱稳定多肽段和大酶的局部区域,可以测量结构动力学和稳定性信息。