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A Fast-Response Red Shifted Fluorescent Probe for Detection of H(2)S in Living Cells
Near-infrared (NIR) fluorescent probes are attractive tools for bioimaging applications because of their low auto-fluorescence interference, minimal damage to living samples, and deep tissue penetration. H(2)S is a gaseous signaling molecule that is involved in redox homeostasis and numerous biologi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036821/ https://www.ncbi.nlm.nih.gov/pubmed/31973081 http://dx.doi.org/10.3390/molecules25030437 |
Sumario: | Near-infrared (NIR) fluorescent probes are attractive tools for bioimaging applications because of their low auto-fluorescence interference, minimal damage to living samples, and deep tissue penetration. H(2)S is a gaseous signaling molecule that is involved in redox homeostasis and numerous biological processes in vivo. To this end, we have developed a new red shifted fluorescent probe 1 to detect physiological H(2)S in live cells. The probe 1 is based on a rhodamine derivative as the red shifted fluorophore and the thiolysis of 7-nitro 1,2,3-benzoxadiazole (NBD) amine as the H(2)S receptor. The probe 1 displays fast fluorescent enhancement at 660 nm (about 10-fold turn-ons, k(2) = 29.8 M(−1)s(−1)) after reacting with H(2)S in buffer (pH 7.4), and the fluorescence quantum yield of the activated red shifted product can reach 0.29. The probe 1 also exhibits high selectivity and sensitivity towards H(2)S. Moreover, 1 is cell-membrane-permeable and mitochondria-targeting, and can be used for imaging of endogenous H(2)S in living cells. We believe that this red shifted fluorescent probe can be a useful tool for studies of H(2)S biology. |
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