The “depict” strategy for discovering new compounds in complex matrices: Lycibarbarspermidines as a case

化学 瓶颈 工作流程 碎片(计算) 管道(软件) 复矩阵 组合化学 色谱法 生物系统 计算机科学 数据库 生物 操作系统 嵌入式系统 程序设计语言
作者
Chao Han,Zhixin Zhang,Zhiyang Feng,Chuanjia Zhai,Xuejiao Li,Yulian Shi,Xiang Li,Miao Li,Ying Wang,Guoan Luo,Xiaoyan Gao
出处
期刊:Journal of Pharmaceutical Analysis [Elsevier]
卷期号:14 (3): 416-426 被引量:1
标识
DOI:10.1016/j.jpha.2023.10.007
摘要

The comprehensive detection and identification of active ingredients in complex matrices is a crucial challenge. Liquid chromatography coupled with high-resolution mass spectrometry (LC-HRMS) is the most prominent analytical platform for the exploration of novel active compounds from complex matrices. However, the LC-HRMS-based analysis workflow suffers from several bottleneck issues, such as trace content of target compounds, limited acquisition for fragment information, and uncertainty in interpreting relevant MS2 spectra. Lycibarbarspermidines are vital antioxidant active ingredients in Lycii Fructus, while the reported structures are merely focused on dicaffeoylspermidines due to their low content. To comprehensively detect the new structures of lycibarbarspermidine derivatives, a "depict" strategy was developed in this study. First, potential new lycibarbarspermidine derivatives were designed according to the biosynthetic pathway, and a comprehensive database was established, which enlarged the coverage of lycibarbarspermidine derivatives. Second, the polarity-oriented sample preparation of potential new compounds increased the concentration of the target compounds. Third, the construction of the molecular network based on the fragmentation pathway of lycibarbarspermidine derivatives broadened the comprehensiveness of identification. Finally, the weak response signals were captured by data-dependent scanning (DDA) followed by parallel reaction monitoring (PRM), and the efficiency of acquiring MS2 fragment ions of target compounds was significantly improved. Based on the integrated strategy above, 210 lycibarbarspermidine derivatives were detected and identified from Lycii Fructus, and in particular, 170 potential new compounds were structurally characterized. The integrated strategy improved the sensitivity of detection and the coverage of low-response components, and it is expected to be a promising pipeline for discovering new compounds.
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