谷胱甘肽
离域电子
化学
亚细胞定位
纳米探针
细胞器
连接器
细胞质
生物物理学
生物化学
纳米技术
材料科学
有机化学
计算机科学
生物
纳米颗粒
操作系统
酶
作者
Longyi Zhu,Bernardino J. Córdova Wong,Yang Li,Hao Xin,Bin Liu,Jianping Lei
标识
DOI:10.1002/chem.201900151
摘要
Abstract Distinguishing glutathione (GSH) level in different subcellular locations is critical for studying its antioxidant function in the signaling system. However, traditional methods for imaging subcellular GSH were achieved in isolated organelles or fixed cells. In this work, we report a quencher‐delocalized emission strategy for in situ profiling of GSH at different subcellular locations in living cells. A nonemissive metal–organic framework (MOF) nanoprobe was designed with AIEgen as the linker and Cu II as the node and quencher. The AIEgen in MOF structure was lightened up with green emission in a neutral environment due to partial Cu II delocalization by competitive binding to GSH. Meanwhile, along with the protonation of AIEgen ligand under acidic environment, the AIEgen‐based MOF could be completely dissociated in the presence of GSH to yield yellow emission. The two‐channel ratiometric analysis of dual‐colored emission of AIEgen‐based MOF allows visualization of GSH in cytoplasm and lysosome in living cells, which is also able to report the drug effects on different subcellular GSH levels.
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