硝基还原酶
化学
菁
细胞内
细菌细胞结构
荧光
活体细胞成像
分析物
酶
细菌
分子探针
生物物理学
生物化学
细胞
荧光寿命成像显微镜
组合化学
色谱法
DNA
生物
物理
量子力学
遗传学
作者
JI Yu-bin,Yali Wang,Na Zhang,Shengnan Xu,Leilei Zhang,Qinghua Wang,Qingyang Zhang,Hai‐Yu Hu
标识
DOI:10.1021/acs.joc.8b02746
摘要
Enzyme-activated fluorogenic probes, which invoke enzymatic catalysis to trigger the generation of fluorescence, provide a versatile platform for monitoring biological processes. The development of fluorogenic probes that can readily penetrate the cell envelopes of bacteria are essential to examine intracellular targets of live bacterial cells. Herein, we present the design, synthesis, properties, and biological applications of two series of fluorogenic probes based on cyanine 5 for identification of bacterial nitroreductase (NTR). The selected fluorogenic probe 3 generates a rapid 10-fold fluorescence response after being catalytically reduced by NTR to the intermediate para-aminobenzyl substituted which then underwent a rearrangement elimination reaction. Moreover, probe 3 is cell permeable for both Gram-positive and Gram-negative bacterial cell envelopes and is selective for NTR over other biological analytes, thus minimizing the background signal and enabling the real-time intracellular imaging of NTR in live bacterial cells.
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