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基于差分迁移谱的心磷脂分析。

Differential Mobility Spectrometry-Based Cardiolipin Analysis.

机构信息

Metabolomics and Proteomics Core, Helmholtz Zentrum München, Neuherberg, Germany.

Chair of Analytical Food Chemistry, TUM School of Life Sciences, Technical University of Munich, Freising-Weihenstephan, Germany.

出版信息

Methods Mol Biol. 2025;2855:373-385. doi: 10.1007/978-1-0716-4116-3_22.

DOI:10.1007/978-1-0716-4116-3_22
PMID:39354319
Abstract

Cardiolipins (CL) are special lipids in many respects. First of all, CL are composed of four fatty acids linked by two phosphatidic acids, which provide CL a unique molecular structure. Secondly, in eukaryotic cells they are specific to a single organelle, mitochondria, where they are also synthetized. CL are one of the most abundant lipid classes in mitochondria, mainly localized in the inner membrane. They are key determinants of mitochondrial health and homeostasis by modulating membrane integrity and fluidity, mitochondrial shapes, and metabolic pathways. Disturbances in mitochondrial CL composition can lead to tissue malfunction and diseases. It is therefore important to develop analytical tools to study the mitochondrial lipidome, and more particularly the CL. The method described here allows the quantification of cardiolipins at the sum composition level in isolated mitochondria or in liver tissue by flow injection analysis coupled to differential mobility spectrometry (FIA-DMS), also known as DMS-based shotgun lipidomics.

摘要

心磷脂(CL)在许多方面都是特殊的脂质。首先,CL 由两条通过两个磷脂酸连接的四个脂肪酸组成,这为 CL 提供了独特的分子结构。其次,在心细胞中,它们是一种细胞器——线粒体的特异性物质,而线粒体也是 CL 的合成部位。CL 是线粒体中最丰富的脂质之一,主要位于内膜中。它们通过调节膜的完整性和流动性、线粒体的形状和代谢途径来成为线粒体健康和动态平衡的关键决定因素。线粒体 CL 组成的紊乱会导致组织功能障碍和疾病。因此,开发分析工具来研究线粒体脂组学,特别是 CL,是非常重要的。本文描述的方法通过流动注射分析与差速迁移谱(FIA-DMS)联用(也称为基于 DMS 的 shotgun 脂质组学),可以在分离的线粒体或肝组织中定量心磷脂的总组成水平。

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本文引用的文献

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Advances in methods to analyse cardiolipin and their clinical applications.分析心磷脂的方法进展及其临床应用
Trends Analyt Chem. 2022 Dec;157:116808. doi: 10.1016/j.trac.2022.116808.
2
Uncovering pathophysiological changes in frontotemporal dementia using serum lipids.利用血清脂质揭示额颞叶痴呆的病理生理变化。
Sci Rep. 2020 Feb 27;10(1):3640. doi: 10.1038/s41598-020-60457-w.
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MITO-Tag Mice enable rapid isolation and multimodal profiling of mitochondria from specific cell types in vivo.MITO-Tag 小鼠可实现从体内特定细胞类型中快速分离和多模式分析线粒体。
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Disentangling oxidation/hydrolysis reactions of brain mitochondrial cardiolipins in pathogenesis of traumatic injury.解析创伤性损伤发病机制中心脑细胞线粒体心磷脂的氧化/水解反应。
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Molecular structural diversity of mitochondrial cardiolipins.线粒体心磷脂的分子结构多样性。
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Mitochondria and Cancer.线粒体与癌症
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Cardiolipin is a key determinant for mtDNA stability and segregation during mitochondrial stress.心磷脂是线粒体应激期间线粒体DNA稳定性和分离的关键决定因素。
Biochim Biophys Acta. 2015 Jun-Jul;1847(6-7):587-98. doi: 10.1016/j.bbabio.2015.03.007. Epub 2015 Apr 2.
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Mammalian cardiolipin biosynthesis.哺乳动物的心磷脂生物合成。
Chem Phys Lipids. 2014 Apr;179:11-6. doi: 10.1016/j.chemphyslip.2013.10.001. Epub 2013 Oct 19.
9
Cytochrome c acts as a cardiolipin oxygenase required for release of proapoptotic factors.细胞色素c作为一种心磷脂加氧酶,是促凋亡因子释放所必需的。
Nat Chem Biol. 2005 Sep;1(4):223-32. doi: 10.1038/nchembio727. Epub 2005 Aug 14.
10
Gluing the respiratory chain together. Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane.将呼吸链整合在一起。线粒体内膜中形成超复合物需要心磷脂。
J Biol Chem. 2002 Nov 15;277(46):43553-6. doi: 10.1074/jbc.C200551200. Epub 2002 Oct 2.