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HILIC-ESI-FTMS with All Ion Fragmentation (AIF) Scans as a Tool for Fast Lipidome Investigations

机译:具有所有离子碎片(AIF)扫描功能的HILIC-ESI-FTMS可作为快速脂质组学研究的工具

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摘要

Lipidomics suffers from the lack of fast and reproducible tools to obtain both structural information on intact phospholipids (PL) and fatty acyl chain composition. Hydrophilic interaction liquid chromatography with electrospray ionization coupled to an orbital-trap Fourier-transform analyzer operating using all ion fragmentation mode (HILIC-ESI-FTMS-AIF MS) is seemingly a valuable resource in this respect. Here, accurate / values, HILIC retention times and AIF MS scan data were combined for PL assignment in standard mixtures or real lipid extracts. AIF scans in both positive and negative ESI mode, achieved using collisional induced dissociation for fragmentation, were applied to identify both the head-group of each PL class and the fatty acyl chains, respectively. An advantage of the AIF approach was the concurrent collection of tandem MS-like data, enabling the identification of linked fatty acyl chains of precursor phospholipids through the corresponding carboxylate anions. To illustrate the ability of AIF in the field of lipidomics, two different types of real samples, i.e., the lipid extracts obtained from human plasma and dermal fibroblasts, were examined. Using AIF scans, a total of 253 intact lipid species and 18 fatty acids across 4 lipid classes were recognized in plasma samples, while FA C20:3 was confirmed as the fatty acyl chain belonging to phosphatidylinositol, PI 38:3, which was found to be down-regulated in fibroblast samples of Parkinson’s disease patients.
机译:脂质组学缺乏获得完整磷脂(PL)和脂肪酰基链组成的结构信息的快速且可复制的工具。在这方面,亲水性相互作用的液相色谱结合电喷雾电离与使用全离子裂解模式运行的轨道阱傅里叶变换分析仪(HILIC-ESI-FTMS-AIF MS)似乎是一种宝贵的资源。在这里,将准确的/值,HILIC保留时间和AIF MS扫描数据结合起来,用于标准混合物或实际脂质提取物中的PL分配。使用碰撞诱导解离进行碎片化,在正和负ESI模式下进行AIF扫描,分别用于识别每个PL类的头基和脂肪酰基链。 AIF方法的优点是可以同时收集串联MS样数据,从而可以通过相应的羧酸根阴离子来鉴定前体磷脂的连接的脂肪酰基链。为了说明AIF在脂质组学领域的能力,检查了两种不同类型的真实样品,即从人血浆和皮肤成纤维细胞获得的脂质提取物。使用AIF扫描,在血浆样品中总共识别了253种完整的脂质种类和4种脂质类别的18种脂肪酸,而FA C20:3被确认为属于磷脂酰肌醇PI 38:3的脂肪酰基链,被发现在帕金森氏病患者的成纤维细胞样本中被下调。

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