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Pseudotargeted Metabolomics Method and Its Application in Serum Biomarker Discovery for Hepatocellular Carcinoma Based on Ultra High-Performance Liquid Chromatography/Triple Quadrupole Mass Spectrometry

机译:基于超高效液相色谱/三重四极杆质谱的伪靶向代谢组学方法及其在肝癌血清生物标志物发现中的应用

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摘要

Untargeted analysis performed using full-scan mass spectrometry (MS) coupled with liquid chromatography (LC) is commonly used in metabolomics. Although they are commonly employed, full-scan MS methods such as quadrupole-time-of-flight (Q-TOF) MS have been restricted by various factors including their limited linear range and complicated data processing. LC coupled with triple quadrupole (QQQ) MS operated in the multiple reaction monitoring (MRM) mode is the gold standard for metabolite quantification; however, only known metabolites are generally quantified, limiting its applications in metabolomic analysis. In this study, a pseudotargeted approach was proposed to perform serum metabolomic analysis using an ultra high-performance liquid chromatography (UHPLC)/QQQ MS system operated in the MRM mode, for which the MRM ion pairs were acquired from the serum samples through untargeted tandem MS using UHPLC/Q-TOF MS. The UHPLC/QQQ MRM MS-based pseudotargeted method displayed better repeatability and wider linear range than the traditional UHPLC/Q-TOF MS-based untargeted metabolomics method, and no complicated peak alignment was required. The developed method was applied to discover serum biomarkers for patients with hepatocellular carcinoma (HCC). Patients with HCC had decreased lysophosphatidylcholine, increased long-chain and decreased medium-chain acylcarnitines, and increased aromatic and decreased branched-chain amino acid levels compared to healthy controls. The novelty of this work is that it provides an approach to acquire MRM ion pairs from real samples, is not limited to metabolite standards, and it provides a foundation to achieve pseudotargeted metabolomic analysis on the widely used LC/QQQ MS platform.
机译:使用全扫描质谱(MS)结合液相色谱(LC)进行的非目标分析通常用于代谢组学。尽管它们通常被使用,但是诸如四极飞行时间(Q-TOF)MS之类的全扫描MS方法受到各种因素的限制,包括其有限的线性范围和复杂的数据处理。在多反应监测(MRM)模式下运行的LC与三重四极杆(QQQ)质谱联用是代谢物定量的金标准;但是,通常仅对已知的代谢物进行定量,从而限制了其在代谢组学分析中的应用。在这项研究中,提出了一种伪靶向方法,该方法使用在MRM模式下运行的超高效液相色谱(UHPLC)/ QQQ MS系统进行血清代谢组学分析,该方法通过非靶向串联从血清样品中获取MRM离子对。使用UHPLC / Q-TOF MS的MS与传统的基于UHPLC / Q-TOF MS的非靶向代谢组学方法相比,基于UHPLC / QQQ MRM MS的伪靶向方法显示出更好的可重复性和更宽的线性范围,并且不需要复杂的峰比对。所开发的方法用于发现肝细胞癌(HCC)患者的血清生物标志物。与健康对照组相比,HCC患者的溶血磷脂酰胆碱含量降低,长链和中链酰基肉碱含量降低,芳香族含量增加,支链氨基酸含量降低。这项工作的新颖性在于,它提供了一种从真实样品中获取MRM离子对的方法,不仅限于代谢物标准品,而且还为在广泛使用的LC / QQQ MS平台上实现伪靶向代谢组学分析提供了基础。

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