Microfluidic Sampling of Undissolved Components from Subcellular Regions of Living Single Cells for Mass Spectrometry Analysis
Precise sampling of undissolved chemical components from subcellular regions of living single cells is a prerequisite for their in-depth analysis, which could promote understanding of subtle early stage physiological or pathological processes. Here we report a microfluidic method to extract undissolved components from subcellular regions for MS analysis. The target single cell was isolated by the microchamber beneath the microfluidic probe and washed by the injected biocompatible isotonic glucose aqueous solution (IGAS). Then, the sampling solvent was injected to extract undissolved components from the expected subcellular region of the living single cell, where the position and size of the sampling region could be controlled. The components immobilized by undissolved cellular structures were proven to be successfully extracted. Since unextracted subcellular regions were protected by IGAS, the single cell could survive after a tiny part was extracted, providing the possibility of repetitive sampling of the same living cell. Phospholipids extracted from the subcellular regions were successfully identified. The results demonstrated the feasibility of our method for subcellular sampling and analysis.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:95 |
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Enthalten in: |
Analytical chemistry - 95(2023), 49 vom: 12. Dez., Seite 18082-18090 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Zhang, Qiang [VerfasserIn] |
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Links: |
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Themen: |
Journal Article |
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Anmerkungen: |
Date Completed 16.12.2023 Date Revised 20.02.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1021/acs.analchem.3c03086 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM365234508 |
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520 | |a Precise sampling of undissolved chemical components from subcellular regions of living single cells is a prerequisite for their in-depth analysis, which could promote understanding of subtle early stage physiological or pathological processes. Here we report a microfluidic method to extract undissolved components from subcellular regions for MS analysis. The target single cell was isolated by the microchamber beneath the microfluidic probe and washed by the injected biocompatible isotonic glucose aqueous solution (IGAS). Then, the sampling solvent was injected to extract undissolved components from the expected subcellular region of the living single cell, where the position and size of the sampling region could be controlled. The components immobilized by undissolved cellular structures were proven to be successfully extracted. Since unextracted subcellular regions were protected by IGAS, the single cell could survive after a tiny part was extracted, providing the possibility of repetitive sampling of the same living cell. Phospholipids extracted from the subcellular regions were successfully identified. The results demonstrated the feasibility of our method for subcellular sampling and analysis | ||
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650 | 4 | |a Research Support, Non-U.S. Gov't | |
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700 | 1 | |a Yi, Xizhen |e verfasserin |4 aut | |
700 | 1 | |a Xie, Tianze |e verfasserin |4 aut | |
700 | 1 | |a Xing, Gaowa |e verfasserin |4 aut | |
700 | 1 | |a Li, Yuxuan |e verfasserin |4 aut | |
700 | 1 | |a Wang, Xiaorui |e verfasserin |4 aut | |
700 | 1 | |a Lin, Jin-Ming |e verfasserin |4 aut | |
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