Center for Mitochondrial Diseases, Case Western Reserve University, Cleveland, OH, USA; Department of Pharmacology, Case Western Reserve University, Cleveland, OH, USA.
Center for Mitochondrial Diseases, Case Western Reserve University, Cleveland, OH, USA; Department of Pharmacology, Case Western Reserve University, Cleveland, OH, USA; Department of Medicine, Case Western Reserve University, Cleveland, OH, USA.
J Lipid Res. 2020 Dec;61(12):1707-1719. doi: 10.1194/jlr.RA120001044. Epub 2020 Sep 30.
Phospholipids, including ether phospholipids, are composed of numerous isomeric and isobaric species that have the same backbone and acyl chains. This structural resemblance results in similar fragmentation patterns by collision-induced dissociation of phospholipids regardless of class, yielding complicated MS/MS spectra when isobaric species are analyzed together. Furthermore, the presence of isobaric species can lead to misassignment of species when made solely based on their molecular weights. In this study, we used normal-phase HPLC for ESI-MS/MS analysis of phospholipids from bovine heart mitochondria. Class separation by HPLC eliminates chances for misidentification of isobaric species from different classes of phospholipids. Chromatography yields simple MS/MS spectra without interference from isobaric species, allowing clear identification of peaks corresponding to fragmented ions containing monoacylglycerol backbone derived from losing one acyl chain. Using these fragmented ions, we characterized individual and isomeric species in each class of mitochondrial phospholipids, including unusual species, such as PS, containing an ether linkage and species containing odd-numbered acyl chains in cardiolipin, PS, PI, and PG. We also characterized monolysocardiolipin and dilysocardiolipin, the least abundant but nevertheless important mitochondrial phospholipids. The results clearly show the power of HPLC-MS/MS for identification and characterization of phospholipids, including minor species.
磷脂,包括醚磷脂,由许多具有相同骨架和酰基链的同分异构体和等规体组成。这种结构上的相似性导致磷脂在碰撞诱导解离时产生相似的碎裂模式,无论磷脂的类别如何,都会产生复杂的 MS/MS 谱,当等规体一起分析时更是如此。此外,等规体的存在可能导致在仅根据分子量进行分配时出现物种错误分配的情况。在本研究中,我们使用正相 HPLC-ESI-MS/MS 分析牛心线粒体中的磷脂。HPLC 的类别分离消除了不同类别磷脂中同分异构体的错误鉴定机会。色谱法产生的 MS/MS 谱简单,不受等规体的干扰,允许清晰地识别对应于失去一个酰基链的单酰基甘油骨架衍生的碎裂离子的峰。使用这些碎裂离子,我们对每种线粒体磷脂的单个和同分异构体进行了特征化,包括含有醚键的 PS 等不寻常的物种以及心磷脂、PS、PI 和 PG 中含有奇数碳酰链的物种。我们还对单酰基心磷脂和二酰基心磷脂进行了特征化,它们是丰度最低但仍然很重要的线粒体磷脂。结果清楚地表明了 HPLC-MS/MS 对磷脂,包括微量物种的鉴定和特征化的强大功能。