Lipidomic Characterization of Oocytes at Single-Cell Level Using Nanoflow Chromatography-Trapped Ion Mobility Spectrometry-Mass Spectrometry.
Pujia ZhuGuowei BuRuifeng HuXianqin RuanRongrong FuZhourui ZhangQiongqiong WanXin LiuYiliang MiaoSuming ChenPublished in: Molecules (Basel, Switzerland) (2023)
Mass spectrometry (MS)-based lipidomic has become a powerful tool for studying lipids in biological systems. However, lipidome analysis at the single-cell level remains a challenge. Here, we report a highly sensitive lipidomic workflow based on nanoflow liquid chromatography and trapped ion mobility spectrometry (TIMS)-MS. This approach enables the high-coverage identification of lipidome landscape at the single-oocyte level. By using the proposed method, comprehensive lipid changes in porcine oocytes during their maturation were revealed. The results provide valuable insights into the structural changes of lipid molecules during porcine oocyte maturation, highlighting the significance of sphingolipids and glycerophospholipids. This study offers a new approach to the single-cell lipidomic.
Keyphrases
- mass spectrometry
- single cell
- liquid chromatography
- gas chromatography
- rna seq
- high resolution
- tandem mass spectrometry
- high resolution mass spectrometry
- solid phase extraction
- high performance liquid chromatography
- high throughput
- capillary electrophoresis
- liquid chromatography tandem mass spectrometry
- simultaneous determination
- fatty acid
- molecularly imprinted
- electronic health record
- high speed
- healthcare