化学
代谢物
色谱法
质谱法
代谢组学
萃取(化学)
注释
液相色谱-质谱法
分辨率(逻辑)
生物化学
人工智能
计算机科学
作者
Fujian Zheng,Lei You,Wangshu Qin,Runze Ouyang,Wangjie Lv,Lei Guo,Xin Lu,Enyou Li,Xinjie Zhao,Guowang Xu
标识
DOI:10.1021/acs.analchem.1c04783
摘要
Liquid chromatography–high-resolution mass spectrometry (LC-HRMS) is the most popular platform for untargeted metabolomics studies, but compound annotation is a challenge. In this work, we developed a new LC-HRMS data-targeted extraction method called MetEx for metabolite annotation. MetEx contains the retention time (tR), MS1, and MS2 information of 30 620 metabolites from freely available spectral databases, including MoNA and KEGG. The tR values of 95.4% of the compounds in our database were calculated by the GNN-RT model. The MS2 spectra of 39.4% compounds were also predicted using CFM-ID. MetEx was initially examined on a mixture of 634 standards, considering chemical coverage and accurate metabolite assignment, and later applied to human plasma (NIST SRM 1950), human urine, HepG2 cells, mouse liver tissue, and mouse feces. MetEx correctly assigned 252 out of 253 standards detected in our instruments. The platform also provided 8.0–44.2% more compounds in the biological samples compared to XCMS, MS-DIAL, and MZmine 2. MetEx is implemented and visualized in R and freely available at http://www.metaboex.cn/MetEx.
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