School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, Jiangsu 211198, China.
School of Pharmacy, Guangdong Pharmaceutical University, Guangdong 510006, China.
Anal Chem. 2023 Aug 29;95(34):12964-12973. doi: 10.1021/acs.analchem.3c02888. Epub 2023 Aug 18.
Metabolomics based on high-resolution mass spectrometry has become a powerful technique in biomedical research. The development of various analytical tools and online libraries has promoted the identification of biomarkers. However, how to make mass spectrometry collect more data information is an important but underestimated research topic. Herein, we combined full-scan and data-dependent acquisition (DDA) modes to develop a new targeted DDA based on the inclusion list of differential and preidentified ions (dpDDA). In this workflow, the MS datasets for statistical analysis and metabolite preidentification were first obtained using full-scan, and then, the MS/MS datasets for metabolite identification were obtained using targeted DDA of quality control samples based on the inclusion list. Compared with the current methods (DDA, data-independent acquisition, targeted DDA with time-staggered precursor ion list, and iterative exclusion DDA), dpDDA showed better stability, higher characteristic ion coverage, higher differential metabolites' MS/MS coverage, and higher quality MS/MS spectra. Moreover, the same trend was verified in the analysis of large-scale clinical samples. More surprisingly, dpDDA can distinguish patients with different severities of coronary heart disease (CHD) based on the Canadian Cardiovascular Society angina classification, which we cannot distinguish through conventional metabolomics data collection. Finally, dpDDA was employed to differentiate CHD from healthy control, and targeted metabolomics confirmed that dpDDA could identify a more complete metabolic pathway network. At the same time, four unreported potential CHD biomarkers were identified, and the area under the receiver operating characteristic curve was greater than 0.85. These results showed that dpDDA would expand the discovery of biomarkers based on metabolomics, more comprehensively explore the key metabolites and their association with diseases, and promote the development of precision medicine.
基于高分辨率质谱的代谢组学已成为生物医学研究中的一种强大技术。各种分析工具和在线文库的发展促进了生物标志物的鉴定。然而,如何使质谱收集更多的数据信息是一个重要但被低估的研究课题。在此,我们结合全扫描和数据依赖采集(DDA)模式,开发了一种基于差异和预鉴定离子(dpDDA)包含列表的新型靶向 DDA。在该工作流程中,首先使用全扫描获得用于统计分析和代谢物预鉴定的 MS 数据集,然后使用基于包含列表的质量控制样品的靶向 DDA 获得用于代谢物鉴定的 MS/MS 数据集。与当前方法(DDA、数据非依赖性采集、基于时间错开的前体离子列表的靶向 DDA 和迭代排除 DDA)相比,dpDDA 显示出更好的稳定性、更高的特征离子覆盖率、更高的差异代谢物的 MS/MS 覆盖率和更高质量的 MS/MS 谱。此外,在对大规模临床样本的分析中也验证了相同的趋势。更令人惊讶的是,dpDDA 可以根据加拿大心血管学会心绞痛分类区分不同严重程度的冠心病(CHD)患者,而我们无法通过常规代谢组学数据采集来区分。最后,dpDDA 用于区分 CHD 与健康对照,靶向代谢组学证实 dpDDA 可以识别更完整的代谢途径网络。同时,鉴定出了四个未报道的潜在 CHD 生物标志物,其接收者操作特征曲线下面积大于 0.85。这些结果表明,dpDDA 将扩展基于代谢组学的生物标志物发现,更全面地探索关键代谢物及其与疾病的关联,并促进精准医学的发展。