A Direct Infusion Probe for Rapid Metabolomics of Low-Volume Samples.
Cátia MarquesLiangwen LiuKyle D DuncanIngela LanekoffPublished in: Analytical chemistry (2022)
Targeted and nontargeted metabolomics has the potential to evaluate and detect global metabolite changes in biological systems. Direct infusion mass spectrometric analysis enables detection of all ionizable small molecules, thus simultaneously providing information on both metabolites and lipids in chemically complex samples. However, to unravel the heterogeneity of the metabolic status of cells in culture and tissue a low number of cells per sample should be analyzed with high sensitivity, which requires low sample volumes. Here, we present the design and characterization of the direct infusion probe, DIP. The DIP is simple to build and position directly in front of a mass spectrometer for rapid metabolomics of chemically complex biological samples using pneumatically assisted electrospray ionization at 1 μL/min flow rate. The resulting data is acquired in a square wave profile with minimal carryover between samples that enhances throughput and enables several minutes of uniform MS signal from 5 μL sample volumes. The DIP was applied to study the intracellular metabolism of insulin secreting INS-1 cells and the results show that exposure to 20 mM glucose for 15 min significantly alters the abundance of several small metabolites, amino acids, and lipids.
Keyphrases
- induced apoptosis
- mass spectrometry
- cell cycle arrest
- low dose
- ms ms
- type diabetes
- loop mediated isothermal amplification
- endoplasmic reticulum stress
- high resolution
- cell death
- machine learning
- amino acid
- drug delivery
- fatty acid
- cancer therapy
- skeletal muscle
- social media
- big data
- climate change
- wastewater treatment
- human health
- antibiotic resistance genes