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调整 Au-MOF 荧光探针的线性范围,用于实时分析活细胞内的 GSH。

Adjusting the Linear Range of Au-MOF Fluorescent Probes for Real-Time Analyzing Intracellular GSH in Living Cells.

机构信息

State Key Laboratory of Bioelectronics (Chien-Shiung Wu Lab), School of Biological Science and Medical Engineering , Southeast University , Nanjing 210096 , China.

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering , Nanjing University , Nanjing 210023 , China.

出版信息

ACS Appl Mater Interfaces. 2018 Apr 18;10(15):12417-12423. doi: 10.1021/acsami.7b19356. Epub 2018 Apr 5.

Abstract

A series of Au-loaded metal-organic frameworks (MOFs) were synthesized in this study and further employed for real-time quantitative analysis of intracellular glutathione (GSH) level. Different linear ranges can be acquired by altering the size of gold and MOF particles, or adjusting the proportion of 2-aminoterephthalic acid/1,4-benzenedicarboxylate linkers, which is also observed on fluorescein isothiocyanate-attached Au-MOFs. Further study reveals that the flexible molecular chain of GSH with the -COOH/-NH and -SH terminals may readily tie on relevant gold nanoparticles through its -NH/-COOH groups, which then restricts the intramolecular motions of fluorescence probes and thus induces marked fluorescence enhancement. On the basis of these observations, the intracellular GSH levels of different cells including L02 cells, Hela, and U87 as well as HepG2 cancer cells can be rapidly evaluated by these Au-MOF probes.

摘要

本研究合成了一系列负载金的金属有机骨架(MOFs),并进一步将其用于实时定量分析细胞内谷胱甘肽(GSH)水平。通过改变金和 MOF 颗粒的大小,或调整 2-氨基对苯二甲酸/1,4-苯二甲酸连接体的比例,可以获得不同的线性范围,在荧光素异硫氰酸酯连接的 Au-MOFs 上也可以观察到这种情况。进一步的研究表明,具有 -COOH/-NH 和 -SH 末端的 GSH 柔性分子链可以通过其 -NH/-COOH 基团轻易地与相关的金纳米粒子结合,从而限制荧光探针的分子内运动,从而导致显著的荧光增强。基于这些观察结果,可以使用这些 Au-MOF 探针快速评估包括 L02 细胞、Hela、U87 以及 HepG2 癌细胞在内的不同细胞内的 GSH 水平。

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