荧光
化学
生物物理学
纳米技术
生物
材料科学
物理
光学
作者
Ismail Ismail,Zhuoyue Chen,Xiuru Ji,Lu Sun,Long Yi,Zhen Xi
出处
期刊:Molecules
[MDPI AG]
日期:2020-01-21
卷期号:25 (3): 437-437
被引量:21
标识
DOI:10.3390/molecules25030437
摘要
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. H2S 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 H2S 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 H2S receptor. The probe 1 displays fast fluorescent enhancement at 660 nm (about 10-fold turn-ons, k2 = 29.8 M-1s-1) after reacting with H2S 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 H2S. Moreover, 1 is cell-membrane-permeable and mitochondria-targeting, and can be used for imaging of endogenous H2S in living cells. We believe that this red shifted fluorescent probe can be a useful tool for studies of H2S biology.
科研通智能强力驱动
Strongly Powered by AbleSci AI