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使用经测定的 MS/MS 谱图库进行氧化磷脂的综合分析。

Comprehensive analyses of oxidized phospholipids using a measured MS/MS spectra library.

机构信息

Laboratory for Metabolomics, RIKEN Center for Integrative Medical Sciences (IMS), Tsurumi, Yokohama, Kanagawa 230-0045, Japan.

Cellular and Molecular Epigenetics Laboratory, Graduate School of Medical Life Science, Yokohama City University, Tsurumi, Yokohama, Kanagawa 230-0045, Japan.

出版信息

J Lipid Res. 2017 Nov;58(11):2229-2237. doi: 10.1194/jlr.D077123. Epub 2017 Sep 5.

Abstract

Oxidized phospholipids (OxPLs) are widely held to be associated with various diseases, such as arteriosclerosis, diabetes, and cancer. To characterize the structure-specific behavior of OxPLs and their physiological relevance, we developed a comprehensive analytical method by establishing a measured MS/MS spectra library of OxPLs. Biogenic OxPLs were prepared by the addition of specific oxidized fatty acids to cultured cells, where they were incorporated into cellular phospholipids, and untargeted lipidomics by LC-quadrupole/TOF-MS was applied to collect MS/MS spectra for the OxPLs. Based on the measured MS/MS spectra for about 400 molecular species of the biogenic OxPLs, we developed a broad-targeted lipidomics system using triple quadrupole MS. Separation precision of structural isomers was optimized by multiple reaction monitoring analysis and this system enabled us to detect OxPLs at levels as low as 10 fmol. When applied to biological samples, i.e., mouse peritoneal macrophages, this system enabled us to monitor a series of OxPLs endogenously produced in a 12/15-lipoxygenase-dependent manner. This advanced analytical method will be useful to elucidate the structure-specific behavior of OxPLs and their physiological relevance in vivo.

摘要

氧化磷脂(OxPLs)被广泛认为与各种疾病有关,如动脉粥样硬化、糖尿病和癌症。为了描述 OxPLs 的结构特异性行为及其生理相关性,我们通过建立 OxPLs 的测量 MS/MS 谱图库,开发了一种全面的分析方法。生物来源的 OxPLs 通过向培养细胞中添加特定的氧化脂肪酸来制备,然后将其掺入细胞磷脂中,并应用 LC-四极杆/TOF-MS 进行非靶向脂质组学分析,以收集 OxPLs 的 MS/MS 谱。基于约 400 种生物来源 OxPLs 的测量 MS/MS 谱,我们使用三重四极杆 MS 开发了一种广泛靶向的脂质组学系统。通过多反应监测分析优化了结构异构体的分离精度,该系统使我们能够检测到低至 10 fmol 的 OxPLs。当应用于生物样本,即小鼠腹腔巨噬细胞时,该系统使我们能够监测 12/15-脂氧合酶依赖性内源性产生的一系列 OxPLs。这种先进的分析方法将有助于阐明 OxPLs 的结构特异性行为及其在体内的生理相关性。

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