谷胱甘肽
生物物理学
内生
细胞内
生物分子
跨膜蛋白
纳米技术
化学
细胞膜
细胞
材料科学
生物化学
生物
受体
酶
作者
Yili Liu,Siyuan Yu,Ruibing An,Yinxing Miao,Dechen Jiang,Deju Ye,Jing‐Juan Xu,Weiwei Zhao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-08-21
卷期号:17 (17): 17468-17475
被引量:22
标识
DOI:10.1021/acsnano.3c05825
摘要
Biological channels can rapidly and continuously modulate ion transport behaviors in response to external stimuli, which play essential roles in manipulating physiological and pathological processes in cells. Here, to mimic the biological channels, a bionic nanochannel is developed by synergizing a cationic silicon-substituted rhodamine (SiRh) with a glass nanopipette for transmembrane single-cell quantification. Taking the fast and reversible nucleophilic addition reaction between glutathione (GSH) and SiRh, the bionic nanochannel shows a fast and reversible response to GSH, with its inner-surface charges changing between positive and negative charges, leading to a distinct and reversible switch in ionic current rectification (ICR). With the bionic nanochannel, spatiotemporal-resolved operation is performed to quantify endogenous GSH in a single cell, allowing for monitoring of intracellular GSH fluctuation in tumor cells upon photodynamic therapy and ferroptosis. Our results demonstrate that it is a feasible tool for in situ quantification of the endogenous GSH in single cells, which may be adapted to addressing other endogenous biomolecules in single cells by usage of other stimuli-responsive probes.
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