An integrated strategy to improve data acquisition and metabolite identification by time-staggered ion lists in UHPLC/Q-TOF MS-based metabolomics

被引:13
作者
Wang, Yang [1 ]
Feng, Ruibing [1 ]
He, Chengwei [1 ]
Su, Huanxing [1 ]
Ma, Huan [2 ]
Wan, Jian-Bo [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Room 6034,Bldg N22,Ave Univ, Taipa 999078, Macao, Peoples R China
[2] Guangdong Acad Med Sci, Guangdong Gen Hosp, Guangdong Cardiovasc Inst, Cardiac Rehabil Dept, Guangzhou, Guangdong, Peoples R China
关键词
Time-staggered ion list; tsMIM; tsDDA; Metabolomics; TRANSGENIC MICE; MASS; INFLAMMATION; RESOLUTION;
D O I
10.1016/j.jpba.2018.05.020
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The narrow linear range and the limited scan time of the given ion make the quantification of the features challenging in liquid chromatography-mass spectrometry (LC-MS)-based untargeted metabolomics with the full-scan mode. And metabolite identification is another bottleneck of untargeted analysis owing to the difficulty of acquiring MS/MS information of most metabolites detected. In this study, an integrated workflow was proposed using the newly established multiple ion monitoring mode with time-staggered ion lists (tsMIM) and target-directed data-dependent acquisition with time-staggered ion lists (tsDDA) to improve data acquisition and metabolite identification in UHPLC/Q-TOF MS-based untargeted metabolomics. Compared to the conventional untargeted metabolomics, the proprosed workflow exhibited the better repeatability before and after data normalization. After selecting features with the significant change by statistical analysis, MS/MS information of all these features can be obtained by tsDDA analysis to facilitate metabolite identification. Using time-staggered ion lists, the workflow is more sensitive in data acquisition, especially for the low-abundant features. Moreover, the metabolites with low abundance tend to be wrongly integrated and triggered by full scan-based untargeted analysis with MSE acquisition mode, which can be greatly improved by the proposed workflow. The integrated workflow was also successfully applied to discover serum biosignatures for the genetic modification of fat-1 in mice, which indicated its practicability and great potential in future metabolomics studies. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 179
页数:9
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