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用于提高化学同位素标记液相色谱-质谱代谢组学分析中代谢物可检测性的分段扫描质谱采集

Segment Scan Mass Spectral Acquisition for Increasing the Metabolite Detectability in Chemical Isotope Labeling Liquid Chromatography-Mass Spectrometry Metabolome Analysis.

作者信息

Wang Chu-Fan, Li Liang

机构信息

Department of Chemistry, University of Alberta, Edmonton, Alberta T6G2G2, Canada.

出版信息

Anal Chem. 2022 Aug 23;94(33):11650-11658. doi: 10.1021/acs.analchem.2c02220. Epub 2022 Aug 4.

Abstract

We report a segmented spectrum scan method using Orbitrap MS in chemical isotope labeling (CIL) liquid chromatography-mass spectrometry (LC-MS) for improving the metabolite detection efficiency. In this method, the full / range is divided into multiple segments with the scanning of each segment to produce multiple narrow-range spectra during the LC data acquisition. These segmented spectra are separately processed to extract the peak pair information with each peak pair arising from a differentially labeled metabolite in the analysis of a mixture of C and C reagent-labeled samples. The sublists of peak pairs are merged to form the final peak pair list from the LC-MS run. Various experimental conditions, including automatic gain control (AGC) values, mass resolutions, segment / widths, number of segments, and total data acquisition time in the LC run, were examined to arrive at an optimal setting in the segment scan for increasing the number of detectable metabolites while maintaining the same analysis time as in the full scan. The optimal method used a segment width of 120 / with 60k resolution for a 16 min CIL LC-MS run. Using dansyl-labeled human urine samples as an example, we demonstrated that this method could detect 5867 peak pairs or metabolites (not features), compared to 3765 peak pairs detectable in a full scan, representing a 56% gain. Out of 5867 peak pairs, 5575 (95.0%) could be identified or mass-matched. The relative quantification accuracy was slightly reduced (81% peak pairs were within ±25% of the expected peak ratio of 1.0 in full, compared to 87% in the full scan) due to the inclusion of more low-abundance peak pairs in the segment scan. The peak ratio measurement precision was not significantly affected by the segment scan. We also showed the increase of the peak pair number detectable from 3843 in the full scan to 7273 (89% gain) using the Orbitrap operated at 120k resolution with a 60 / segment width when multiple repeat sample injections were used. Thus, segment scan Orbitrap MS is an enabling method for detecting coeluting metabolites in CIL LC-MS for increasing the metabolomic coverage.

摘要

我们报告了一种在化学同位素标记(CIL)液相色谱 - 质谱联用(LC - MS)中使用轨道阱质谱仪的分段光谱扫描方法,以提高代谢物检测效率。在该方法中,全范围被划分为多个段,在液相色谱数据采集期间对每个段进行扫描以产生多个窄范围光谱。这些分段光谱被分别处理以提取峰对信息,每个峰对来自在分析碳 - 13(¹³C)和碳 - 12(¹²C)试剂标记样品混合物时差异标记的代谢物。峰对的子列表被合并以形成来自LC - MS运行的最终峰对列表。研究了各种实验条件,包括自动增益控制(AGC)值、质量分辨率、段宽、段数以及液相色谱运行中的总数据采集时间,以在分段扫描中达到最佳设置,在保持与全扫描相同分析时间的同时增加可检测代谢物的数量。最佳方法在16分钟的CIL LC - MS运行中使用120 m/z的段宽和60k的分辨率。以丹磺酰标记的人尿样为例,我们证明该方法可检测到5867个峰对或代谢物(而非特征峰),相比之下全扫描中可检测到3765个峰对,增益为56%。在5867个峰对中,5575个(95.0%)可被鉴定或进行质量匹配。由于在分段扫描中包含了更多低丰度峰对,相对定量准确性略有降低(全扫描中87%的峰对在预期峰比1.0的±25%范围内,而分段扫描中为81%)。峰比测量精度未受到分段扫描的显著影响。我们还表明,当使用多次重复进样时,在120k分辨率和60 m/z段宽下运行的轨道阱质谱仪可使可检测峰对数量从全扫描中的3843个增加到7273个(增益89%)。因此,分段扫描轨道阱质谱是一种用于在CIL LC - MS中检测共洗脱代谢物以增加代谢组覆盖范围的有效方法。

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