化学
质谱法
纳米-
电喷雾电离
电喷雾质谱
电喷雾
溶解
接口(物质)
分析化学(期刊)
电离
色谱法
萃取电喷雾电离
灵敏度(控制系统)
蛋白质质谱法
离子
化学工程
有机化学
分子
生物化学
工程类
吉布斯等温线
电子工程
作者
Kanchana Pandian,L. Matos,Laura Ann Hetzel,Raphaël Zwier,Peter J. Van Veldhuizen,Cornelius Schubert,K. S. Jayaprakash,Amy C. Harms,Ahmed Ali,Thomas Hankemeier
标识
DOI:10.1016/j.aca.2024.343068
摘要
Live single-cell metabolomic studies encounter inherent difficulties attributed to the limited sample volume, minimal compound quantity, and insufficient sensitivity in the Mass Spectrometry (MS) method used to obtain single-cell data. However, understanding cellular heterogeneity, functional diversity, and metabolic processes within individual cells is essential. Exploring how individual cells respond to stimuli, including drugs, environmental changes, or signaling molecules, offers insights into biology, oncology, and drug discovery. Efficient release of cell contents (lysis) is vital for accurate metabolite detection at the single-cell level. Despite this, traditional approaches in live single cell metabolomics methods do not emphasize efficient lysis to prevent sample dilution. Instead, current live single cell metabolomics methods use direct infusion to introduce the cell into the mass spectrometry without prior chromatographic separation or a lysis step, which adversely affects sensitivity and metabolic coverage.
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