State Key Laboratory of Biocontrol, South China Sea Bio-Resource Exploitation and Utilization Collaborative Innovation Center, School of Life Sciences , Sun Yat-Sen University , 135 Xingangxi Road , Guangzhou 510275 , China.
Guangdong Engineering and Technology Research Center for Ambient Mass Spectrometry, Guangdong Provincial Key Laboratory of Emergency Test for Dangerous Chemicals , Guangdong Institute of Analysis (China National Analytical Center Guangzhou) , 100 Xianlie Middle Road , Guangzhou 510070 , China.
Anal Chem. 2018 Jun 5;90(11):6936-6944. doi: 10.1021/acs.analchem.8b01218. Epub 2018 May 9.
Lipidomics is a significant way to understand the structural and functional roles that lipids play in biological systems. Although many mass spectrometry (MS)-based lipidomics strategies have recently achieve remarkable results, in vivo, in situ, and microscale lipidomics for small biological organisms and cells have not yet been obtained. In this article, we report a novel lipidomics methodology for in vivo, in situ, and microscale investigation of small biological organisms and cells using biocompatible surface-coated probe nanoelectrospray ionization mass spectrometry (BSCP-nanoESI-MS). A novel biocompatible surface-coated solid-phase microextration (SPME) probe is prepared, which possesses a probe-end diameter of less than 5 μm and shows excellent enrichment capacity toward lipid species. In vivo extraction of living biological organisms (e.g., zebrafishes), in situ sampling a precise position of small organisms (e.g., Daphnia magna), and even microscale analysis of single eukaryotic cells (e.g., HepG2) are easily achieved by the SPME probe. After extraction, the loaded SPME probe is directly applied for nanoESI-MS analysis, and a high-resolution mass spectrometer is employed for recording spectra and identifying lipid species. Compared with the conventional direct infusion shotgun MS lipidomics, our proposed methodology shows a similar result of lipid profiles but with simpler sample pretreatment, less sample consumption, and shorter analytical times. Lipidomics of zebrafish, Daphnia magna, and HepG2 cell populations were investigated by our proposed BSCP-nanoESI-MS methodology, and abundant lipid compositions were detected and identified and biomarkers were obtained via multivariate statistical analysis.
脂质组学是了解脂质在生物系统中结构和功能作用的重要方法。尽管最近许多基于质谱(MS)的脂质组学策略已经取得了显著的成果,但对于小型生物和细胞的体内、原位和微观脂质组学尚未实现。在本文中,我们报告了一种使用生物相容性表面涂层探针纳喷雾电离质谱(BSCP-nanoESI-MS)进行小型生物和细胞体内、原位和微观研究的新型脂质组学方法。我们制备了一种新型的生物相容性表面涂层固相微萃取(SPME)探针,其探针端直径小于 5μm,对脂质具有优异的富集能力。通过 SPME 探针可以轻松实现对活体生物(例如斑马鱼)的体内提取、对小型生物(例如大型溞)的精确位置的原位采样,甚至对单个真核细胞(例如 HepG2 细胞)的微尺度分析。提取后,加载的 SPME 探针可直接用于 nanoESI-MS 分析,并使用高分辨率质谱仪记录光谱和鉴定脂质种类。与传统的直接进样 shotgun MS 脂质组学相比,我们提出的方法显示出相似的脂质图谱结果,但具有更简单的样品预处理、更少的样品消耗和更短的分析时间。通过我们提出的 BSCP-nanoESI-MS 方法研究了斑马鱼、大型溞和 HepG2 细胞群体的脂质组学,检测并鉴定了丰富的脂质组成,并通过多变量统计分析获得了生物标志物。