Department of Medicinal Chemistry, University of Washington, Seattle, Washington 98195, United States.
Department of Chemistry & Chemical Biology, Northeastern University, Boston, Massachusetts 02115, United States.
Chem Rev. 2022 Apr 27;122(8):7562-7623. doi: 10.1021/acs.chemrev.1c00279. Epub 2021 Sep 7.
Solution-phase hydrogen/deuterium exchange (HDX) coupled to mass spectrometry (MS) is a widespread tool for structural analysis across academia and the biopharmaceutical industry. By monitoring the exchangeability of backbone amide protons, HDX-MS can reveal information about higher-order structure and dynamics throughout a protein, can track protein folding pathways, map interaction sites, and assess conformational states of protein samples. The combination of the versatility of the hydrogen/deuterium exchange reaction with the sensitivity of mass spectrometry has enabled the study of extremely challenging protein systems, some of which cannot be suitably studied using other techniques. Improvements over the past three decades have continually increased throughput, robustness, and expanded the limits of what is feasible for HDX-MS investigations. To provide an overview for researchers seeking to utilize and derive the most from HDX-MS for protein structural analysis, we summarize the fundamental principles, basic methodology, strengths and weaknesses, and the established applications of HDX-MS while highlighting new developments and applications.
溶液相氢/氘交换(HDX)与质谱(MS)相结合,是学术界和生物制药行业中广泛用于结构分析的工具。通过监测骨架酰胺质子的可交换性,HDX-MS 可以揭示蛋白质整体的高级结构和动力学信息,可跟踪蛋白质折叠途径、绘制相互作用位点,并评估蛋白质样品的构象状态。氢/氘交换反应的多功能性与质谱的灵敏度相结合,使研究极具挑战性的蛋白质系统成为可能,其中一些系统无法使用其他技术进行适当研究。过去三十年来的改进不断提高了通量、稳健性,并扩展了 HDX-MS 研究的可行性极限。为了为寻求利用 HDX-MS 进行蛋白质结构分析并从中获得最大收益的研究人员提供概述,我们总结了 HDX-MS 的基本原理、基本方法、优缺点以及既定的应用,同时强调了新的发展和应用。