Single-Cell Metabolomics with Rapid Determination of Chemical Formulas from Isotopic Fine Structures.
Laith Z SamarahAkos VertesChristopher R AndertonPublished in: Methods in molecular biology (Clifton, N.J.) (2022)
Metabolomic measurements can provide functional readouts of cellular states and phenotypes. Here, we present a protocol for single-cell metabolomics that permits direct untargeted detection of a broad number of metabolites under ambient conditions, without the need for sample processing, and with high confidence in the discovery and identification of the molecular formulas for detected metabolites. This protocol describes combining fiber-based laser ablation electrospray ionization (f-LAESI) with a 21 Tesla Fourier transform ion cyclotron resonance mass spectrometer (21T-FTICR-MS) to obtain high confidence molecular formula information about detected metabolites. The f-LAESI source utilizes mid-infrared laser ablation through a sharp optical fiber tip, affording direct ambient analysis of cells without the need for sample processing. Using the 21T-FTICR-MS as a mass analyzer enabled measurement of the isotopic fine structure (IFS) for numerous metabolites simultaneously from single cells, and the IFSs were in turn computationally processed to rapidly determine the corresponding elemental compositions. This metabolomics technique complements other single cell omics measurement methods, helping to resolve complex molecular interactions that take place within cells unattainable from single cell transcriptomic and proteomics methods.
Keyphrases
- single cell
- mass spectrometry
- ms ms
- rna seq
- induced apoptosis
- air pollution
- high throughput
- cell cycle arrest
- high resolution
- randomized controlled trial
- particulate matter
- multiple sclerosis
- magnetic resonance
- endoplasmic reticulum stress
- oxidative stress
- social media
- radiofrequency ablation
- atrial fibrillation
- fluorescent probe
- health information
- catheter ablation
- gas chromatography mass spectrometry
- quantum dots