Proteinase K Combining Two-Step Liquid–Liquid Extraction for Plasma Untargeted Liquid Chromatography–Mass Spectrometry-Based Metabolomics To Discover the Potential Mechanism of Colorectal Adenoma

化学 代谢组 色谱法 代谢物 代谢组学 萃取(化学) 蛋白质沉淀 样品制备 高效液相色谱法 质谱法 液相色谱-质谱法 生物化学
作者
Qisong Zhang,Yanying Nong,Zhongqiu Liu,Lingzhi Gong
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:91 (22): 14458-14466 被引量:38
标识
DOI:10.1021/acs.analchem.9b03121
摘要

LC-MS-based untargeted metabolomics have been proven to be an extremely promising technique to discover biomarkers and explore the mechanisms underlying diseases, which, however, relies heavily on sample pretreatment for metabolite extraction. In the present study, a systematic and pragmatic evaluation of eight protocols employing conventional metabolites extraction strategies, protein precipitation (PPT), and liquid-liquid extraction (LLE), with and without proteinase K (PK) incubation, was performed simultaneously, using human plasma and a mixture of 39 endogenous metabolite standards. These protocols were as follows: (1) PPT with methanol, (2) PPT with acetonitrile, (3) PPT with 2-propanol, (4) two-step LLE of CH2Cl2-MeOH, followed by MeOH-H2O, (5) PK incubation combining two-step LLE of CH2Cl2-MeOH followed by MeOH-H2O, (6) two-step LLE of CHCl3-MeOH, followed by MeOH-H2O, (7) PK incubation combining two-step LLE of CHCl3-MeOH, followed by MeOH-H2O, (8) PK incubation combining MeOH-EtOH PPT. The results suggested that two-step LLE produced broader metabolome coverage than protein precipitation, and the addition of proteinase K enhanced the extraction performance further. Taken together, PK incubation combining two-step LLE of CHCl3-MeOH, followed by MeOH-H2O, was determined to be the most suitable extraction method, because of its broad metabolome coverage, high reproducibility, and satisfactory recovery. Next, the developed optimal sample preparation method was applied successfully to profile the plasma metabolome of colorectal adenoma and uncover its potential mechanism for significant differential changes in linoleic acid and phospholipid metabolism.
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