Quantitative Hydrogen/Deuterium Exchange Mass Spectrometry

被引:12
|
作者
Hamuro, Yoshitomo [1 ,2 ]
机构
[1] ExSAR Corp, Monmouth Jct, NJ 08852 USA
[2] Janssen Res & Dev LLC, 1400 McKean Rd, Spring House, PA 19477 USA
关键词
hydrogen/deuterium exchange; isotope envelope; mass spectrometry; quantitative; PROTEIN HYDROGEN-EXCHANGE; DEUTERIUM EXCHANGE; PROTEOLYTIC FRAGMENTATION; CONFORMATIONAL DYNAMICS; STRUCTURAL DYNAMICS; TIME WINDOW; RESOLUTION; STABILITY; ANTIBODY; BINDING;
D O I
10.1021/jasms.1c00216
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This Account describes considerations for the data generation, data analysis, and data interpretation of a hydrogen/deuterium exchange-mass spectrometry (HDX-MS) experiment to have a quantitative argument. Although HDX-MS has gained its popularity as a biophysical tool, the argument from its data often remains qualitative. To generate HDX-MS data that are more suitable for a quantitative argument, the sequence coverage and sequence resolution should be optimized during the feasibility stage, and the time window coverage and time window resolution should be improved during the HDX stage. To extract biophysically meaningful values for a certain perturbation from medium-resolution HDX-MS data, there are two major ways: (i) estimating the area between the two deuterium buildup curves using centroid values with and without the perturbation when plotted against log time scale and (ii) dissecting into multiple single-exponential curves using the isotope envelopes. To have more accurate arguments for an HDX-MS perturbation study, (i) false negatives due to sequence coverage, (ii) false negatives due to time window coverage, (iii) false positives due to sequence resolution, and (iv) false positives due to allosteric effects should be carefully examined.
引用
收藏
页码:2711 / 2727
页数:17
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