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石墨烯量子点增强飞行时间二次离子质谱法用于单细胞成像。

Graphene quantum dots enhanced ToF-SIMS for single-cell imaging.

机构信息

Key Laboratory of Advanced Materials, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, China.

出版信息

Anal Bioanal Chem. 2019 Jul;411(18):4025-4030. doi: 10.1007/s00216-019-01686-5. Epub 2019 Feb 22.

Abstract

Time-of-flight secondary ion mass spectrometry (ToF-SIMS) has shown promising applications in single-cell analysis owing to its high spatial resolution molecular imaging capability. One of the main drawbacks hindering progress in this field is the relatively low ionization efficiency for biological systems. The complex chemical micro-environment in single cells typically causes severe matrix effects, leading to significant signal suppression of biomolecules. In this work, we investigated the signal enhancement effect of graphene quantum dots (GE QDs) in ToF-SIMS analysis. A × 160 magnification of ToF-SIMS signal for amiodarone casted on glass slide was observed by adding amino-functionalized GE QDs (amino-GE QDs), which was significantly higher than adding previously reported signal enhancement materials and hydroxyl group-functionalized GE QDs (hydroxyl-GE QDs). A possible mechanism for GE QD-induced signal enhancement was proposed. Further, effects of amino-GE QDs and hydroxyl-GE QDs on amiodarone-treated breast cancer cells were compared. A significant signal improvement for lipids and amiodarone was achieved using both types of GE QDs, especially for amino-GE QDs. In addition, ToF-SIMS chemical mapping of single cells with better quality was obtained after signal enhancement. Our strategy for effective ToF-SIMS signal enhancement holds great potential for further investigation of drug metabolism pathways and the interactions between the cell and micro-environment.

摘要

飞行时间二次离子质谱(ToF-SIMS)因其具有高空间分辨率的分子成像能力,在单细胞分析中显示出了有前景的应用。阻碍该领域发展的一个主要缺点是生物体系的电离效率相对较低。单细胞中复杂的化学微环境通常会导致严重的基质效应,从而导致生物分子的信号显著抑制。在这项工作中,我们研究了石墨烯量子点(GE QD)在 ToF-SIMS 分析中的信号增强效应。通过添加氨基功能化的 GE QD(氨基-GE QD),观察到在玻璃载玻片上浇铸的胺碘酮的 ToF-SIMS 信号放大了 ×160 倍,这明显高于添加以前报道的信号增强材料和羟基功能化的 GE QD(羟基-GE QD)。提出了 GE QD 诱导信号增强的可能机制。此外,还比较了氨基-GE QD 和羟基-GE QD 对胺碘酮处理的乳腺癌细胞的影响。两种类型的 GE QD 都能显著改善脂质和胺碘酮的信号,尤其是氨基-GE QD。此外,经过信号增强后,还获得了具有更好质量的单细胞 ToF-SIMS 化学映射。我们的有效 ToF-SIMS 信号增强策略对于进一步研究药物代谢途径以及细胞与微环境之间的相互作用具有很大的潜力。

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