HeuSMA:改进非靶向代谢组学峰识别的多梯度 LC-MS 策略

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Yao-Yu Chen, Na An, Yan-Zhen Wang, Peng-Cheng Mei, Jun-Di Hao, Song-Mei Liu, Quan-Fei Zhu* and Yu-Qi Feng*, 
{"title":"HeuSMA:改进非靶向代谢组学峰识别的多梯度 LC-MS 策略","authors":"Yao-Yu Chen,&nbsp;Na An,&nbsp;Yan-Zhen Wang,&nbsp;Peng-Cheng Mei,&nbsp;Jun-Di Hao,&nbsp;Song-Mei Liu,&nbsp;Quan-Fei Zhu* and Yu-Qi Feng*,&nbsp;","doi":"10.1021/acs.analchem.4c0531510.1021/acs.analchem.4c05315","DOIUrl":null,"url":null,"abstract":"<p >Metabolomics, which involves the comprehensive analysis of small molecules within biological systems, plays a crucial role in elucidating the biochemical underpinnings of physiological processes and disease conditions. However, current coverage of the metabolome remains limited. In this study, we present a heuristic strategy for untargeted metabolomics analysis (HeuSMA) based on multiple chromatographic gradients to enhance the metabolome coverage in untargeted metabolomics. This strategy involves performing LC-MS analysis under multiple gradient conditions on a given sample (e.g., a pooled sample or a quality control sample) to obtain a comprehensive metabolomics data set, followed by constructing a heuristic peak list using a retention index system. Guided by this list, heuristic peak picking in quantitative metabolomics data is achieved. The benchmarking and validation results demonstrate that HeuSMA outperforms existing tools (such as MS-DIAL and MZmine) in terms of metabolite coverage and peak identification accuracy. Additionally, HeuSMA improves the accessibility of MS/MS data, thereby facilitating the metabolite annotation. The effectiveness of the HeuSMA strategy was further demonstrated through its application in serum metabolomics analysis of human hepatocellular carcinoma (HCC). To facilitate the adoption of the HeuSMA strategy, we also developed two user-friendly graphical interface software solutions (HPLG and HP), which automate the analysis process, enabling researchers to efficiently manage data and derive meaningful conclusions (https://github.com/Lacterd/HeuSMA).</p>","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"97 14","pages":"7719–7728 7719–7728"},"PeriodicalIF":6.7000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"HeuSMA: A Multigradient LC-MS Strategy for Improving Peak Identification in Untargeted Metabolomics\",\"authors\":\"Yao-Yu Chen,&nbsp;Na An,&nbsp;Yan-Zhen Wang,&nbsp;Peng-Cheng Mei,&nbsp;Jun-Di Hao,&nbsp;Song-Mei Liu,&nbsp;Quan-Fei Zhu* and Yu-Qi Feng*,&nbsp;\",\"doi\":\"10.1021/acs.analchem.4c0531510.1021/acs.analchem.4c05315\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Metabolomics, which involves the comprehensive analysis of small molecules within biological systems, plays a crucial role in elucidating the biochemical underpinnings of physiological processes and disease conditions. However, current coverage of the metabolome remains limited. In this study, we present a heuristic strategy for untargeted metabolomics analysis (HeuSMA) based on multiple chromatographic gradients to enhance the metabolome coverage in untargeted metabolomics. This strategy involves performing LC-MS analysis under multiple gradient conditions on a given sample (e.g., a pooled sample or a quality control sample) to obtain a comprehensive metabolomics data set, followed by constructing a heuristic peak list using a retention index system. Guided by this list, heuristic peak picking in quantitative metabolomics data is achieved. The benchmarking and validation results demonstrate that HeuSMA outperforms existing tools (such as MS-DIAL and MZmine) in terms of metabolite coverage and peak identification accuracy. Additionally, HeuSMA improves the accessibility of MS/MS data, thereby facilitating the metabolite annotation. The effectiveness of the HeuSMA strategy was further demonstrated through its application in serum metabolomics analysis of human hepatocellular carcinoma (HCC). To facilitate the adoption of the HeuSMA strategy, we also developed two user-friendly graphical interface software solutions (HPLG and HP), which automate the analysis process, enabling researchers to efficiently manage data and derive meaningful conclusions (https://github.com/Lacterd/HeuSMA).</p>\",\"PeriodicalId\":27,\"journal\":{\"name\":\"Analytical Chemistry\",\"volume\":\"97 14\",\"pages\":\"7719–7728 7719–7728\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.analchem.4c05315\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.analchem.4c05315","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

代谢组学涉及对生物系统内小分子的综合分析,在阐明生理过程和疾病条件的生化基础方面起着至关重要的作用。然而,目前对代谢组的覆盖范围仍然有限。在这项研究中,我们提出了一种基于多重色谱梯度的非靶向代谢组学分析(HeuSMA)的启发式策略,以提高非靶向代谢组学的代谢组学覆盖率。该策略包括在给定样品(例如,合并样品或质量控制样品)的多个梯度条件下进行LC-MS分析,以获得全面的代谢组学数据集,然后使用保留指数系统构建启发式峰列表。在此列表的指导下,实现了定量代谢组学数据的启发式峰值选取。基准测试和验证结果表明,HeuSMA在代谢物覆盖率和峰识别准确性方面优于现有工具(如MS-DIAL和MZmine)。此外,HeuSMA提高了MS/MS数据的可访问性,从而促进了代谢物的注释。HeuSMA策略的有效性通过其在人肝细胞癌(HCC)血清代谢组学分析中的应用得到进一步证明。为了促进HeuSMA策略的采用,我们还开发了两种用户友好的图形界面软件解决方案(HPLG和HP),使分析过程自动化,使研究人员能够有效地管理数据并得出有意义的结论(https://github.com/Lacterd/HeuSMA)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

HeuSMA: A Multigradient LC-MS Strategy for Improving Peak Identification in Untargeted Metabolomics

HeuSMA: A Multigradient LC-MS Strategy for Improving Peak Identification in Untargeted Metabolomics

Metabolomics, which involves the comprehensive analysis of small molecules within biological systems, plays a crucial role in elucidating the biochemical underpinnings of physiological processes and disease conditions. However, current coverage of the metabolome remains limited. In this study, we present a heuristic strategy for untargeted metabolomics analysis (HeuSMA) based on multiple chromatographic gradients to enhance the metabolome coverage in untargeted metabolomics. This strategy involves performing LC-MS analysis under multiple gradient conditions on a given sample (e.g., a pooled sample or a quality control sample) to obtain a comprehensive metabolomics data set, followed by constructing a heuristic peak list using a retention index system. Guided by this list, heuristic peak picking in quantitative metabolomics data is achieved. The benchmarking and validation results demonstrate that HeuSMA outperforms existing tools (such as MS-DIAL and MZmine) in terms of metabolite coverage and peak identification accuracy. Additionally, HeuSMA improves the accessibility of MS/MS data, thereby facilitating the metabolite annotation. The effectiveness of the HeuSMA strategy was further demonstrated through its application in serum metabolomics analysis of human hepatocellular carcinoma (HCC). To facilitate the adoption of the HeuSMA strategy, we also developed two user-friendly graphical interface software solutions (HPLG and HP), which automate the analysis process, enabling researchers to efficiently manage data and derive meaningful conclusions (https://github.com/Lacterd/HeuSMA).

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信