谷胱甘肽
内生
化学
生物物理学
荧光
纳米传感器
细胞生物学
生物化学
纳米技术
酶
生物
材料科学
量子力学
物理
作者
Xin Mao,Peiyan Yuan,Changmin Yu,Lin Li,Shao Q. Yao
标识
DOI:10.1002/ange.201806710
摘要
Abstract Changes in the cellular levels of glutathione (GSH) and protein S‐glutathionylation (PSSG) are closely associated with a number of human diseases. Despite recent advances, few thiol‐reactive, small‐molecule GSH sensors could selectively detect GSH over other endogenous thiols, and none was capable of detecting PSSG in live mammalian cells. By using a dye‐loaded mesoporous silica nanoquencher (qMSN) capped with anti‐GSH antibody capable of highly selective binding toward GSH and glutathionylated proteins over other molecules, we have successfully developed a fluorescence GSH/PSSG nanosensor, which showed unprecedented selectivity toward PSSG even in the presence of GSH, had amplifiable and programmable fluorescence Turn‐ON properties, and could be used to image endogenous PSSG in live mammalian cells under stimulated conditions for the first time.
科研通智能强力驱动
Strongly Powered by AbleSci AI