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Nanoquencher‐Based Selective Imaging of Protein Glutathionylation in Live Mammalian Cells
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 o...
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Published in: | Angewandte Chemie International Edition 2018-08, Vol.57 (32), p.10257-10262 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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.
Selective detection: By using a mesoporous silica nanoquencher capped with anti‐glutathione‐S‐transferase antibody, a fluorescence nanosensor has been developed. The nanosensor is capable of selectively imaging endogenous protein glutathionylation from live mammalian cells under stimulated conditions. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201806710 |