Department of Chemistry, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
Anal Chem. 2022 Jul 26;94(29):10314-10319. doi: 10.1021/acs.analchem.2c02073. Epub 2022 Jul 13.
Protein footprinting is a mass spectrometry (MS)-based approach to measure protein conformational changes. One approach, specific amino acid labeling, imparts often an irreversible modification to protein side chains but requires careful selection of the reactive reagent and often time-consuming optimization of experimental parameters prior to submission to bottom-up MS analysis. In this work, we repurpose a hydrogen-deuterium exchange MS (HDX-MS) LEAP HDX system for automated specific amino acid footprinting MS, demonstrating its efficacy in reaction optimization and monitoring applicability to specific ligand binding systems. We screened reagent conditions for two model ligand-binding systems and demonstrate the method's efficacy for measuring differences induced by ligand binding. Our proof-of-concept experiments provide a platform for rapidly screening specific amino acid reagents and reaction conditions for protein systems to be studied by footprinting.
蛋白质足迹分析是一种基于质谱(MS)的方法,用于测量蛋白质构象变化。一种方法是特异性氨基酸标记,它通常会对蛋白质侧链进行不可逆的修饰,但需要仔细选择反应试剂,并在进行自上而下的 MS 分析之前,经常需要花费时间优化实验参数。在这项工作中,我们重新利用了氢氘交换 MS(HDX-MS)LEAP HDX 系统进行自动化特异性氨基酸足迹 MS,证明了它在反应优化和监测特定配体结合系统适用性方面的有效性。我们筛选了两种模型配体结合系统的试剂条件,并证明了该方法测量配体结合诱导的差异的功效。我们的概念验证实验为快速筛选要通过足迹分析研究的蛋白质系统的特异性氨基酸试剂和反应条件提供了一个平台。