Single-Cell and Subcellular Analysis Using Ultrahigh Resolution 21 T MALDI FTICR Mass Spectrometry
Daniel C Castro1,2, Karl W Smith3, Miles D Norsworthy2,4
1Department of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, 505 South Goodwin Avenue, Urbana, Illinois 61801, United States.
This study used ultrahigh-resolution mass spectrometry to analyze lipids in individual mammalian brain cells. Researchers identified unique lipid profiles in different cell parts, advancing single-cell lipidomics.
Area of Science:
- Neuroscience
- Lipidomics
- Mass Spectrometry
Background:
- The mammalian brain has a complex lipidome crucial for cell structure and function.
- Cellular lipid profiles change with signals and environment, altering cell phenotype.
- Analyzing individual cell lipidomics is challenging due to sample limitations and lipid diversity.
Purpose of the Study:
- To perform chemical characterization of individual hippocampal cells at ultrahigh mass resolution.
- To demonstrate the capability of high-field Fourier-transform ion cyclotron resonance (FTICR) mass spectrometry for single-cell lipid analysis.
Main Methods:
- Utilized a 21 T FTICR mass spectrometer for ultrahigh mass resolution analysis.
- Applied mass spectrometry (MS) to analyze lipids from individual hippocampal cells.
- Differentiated between freshly isolated and cultured hippocampal cell populations.
Main Results:
- Achieved accurate lipid profiling of individual mammalian cells.
- Identified distinct lipid profiles between cell bodies (soma) and neuronal processes.
- Detected specific lipids like TG 42:2 in cell bodies and SM 34:1;O2 in cellular processes.
Conclusions:
- This work is the first to analyze mammalian single cells at ultrahigh mass resolution using FTICR-MS.
- Ultrahigh resolution MS significantly advances the performance and potential of single-cell lipid research.
- The findings highlight the spatial heterogeneity of lipid distribution within single neurons.
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