Profiling Intact Glycosphingolipids with Automated Structural Annotation and Quantitation from Human Samples with Nanoflow Liquid Chromatography Mass Spectrometry.
Ryan L SchindlerArmin OloumiJennyfer TenaMichael Russelle S AlvarezYiyun LiuSheryl GrijaldoMariana BarbozaLee-Way JinAngela M ZivkovicCarlito B LebrillaPublished in: Analytical chemistry (2024)
Sphingolipids are an essential subset of bioactive lipids found in most eukaryotic cells that contribute to membrane biophysical properties and are involved in cellular differentiation, recognition, and mediating interactions. The described nanoHPLC-ESI-Q/ToF methodology utilizes known biosynthetic pathways, accurate mass detection, optimized collision-induced disassociation, and a robust nanoflow chromatographic separation for the analysis of intact sphingolipids found in human tissue, cells, and serum. The methodology was developed and validated with an emphasis on addressing the common issues experienced in profiling these amphipathic lipids, which are part of the glycocalyx and lipidome. The high sensitivity obtained using nanorange flow rates with robust chromatographic reproducibility over a wide range of concentrations and injection volumes results in confident identifications for profiling these low-abundant biomolecules.
Keyphrases
- mass spectrometry
- liquid chromatography
- simultaneous determination
- induced apoptosis
- liquid chromatography tandem mass spectrometry
- ms ms
- tandem mass spectrometry
- high resolution mass spectrometry
- endothelial cells
- cell cycle arrest
- high performance liquid chromatography
- single cell
- high resolution
- gas chromatography
- solid phase extraction
- induced pluripotent stem cells
- endoplasmic reticulum stress
- signaling pathway
- fatty acid
- diabetic rats
- machine learning
- deep learning
- oxidative stress
- pluripotent stem cells
- drug induced
- cell proliferation
- stress induced
- quantum dots
- sensitive detection