School of Life and Environment Sciences , Harbin University of Commerce , Harbin 150076 , China.
State Key Laboratory of Bioactive Substances and Function of Natural Medicine, Institute of Materia Medica , Chinese Academy of Medical Sciences & Peking Union Medical College , Beijing 100050 , China.
J Org Chem. 2019 Feb 1;84(3):1299-1309. doi: 10.1021/acs.joc.8b02746. Epub 2019 Jan 11.
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.
酶激活荧光探针通过酶催化触发荧光的产生,为监测生物过程提供了一个通用的平台。开发能够轻易穿透细菌细胞膜的荧光探针对于研究活细菌细胞内的靶标至关重要。在此,我们设计、合成了基于菁染料 5 的两类用于鉴定细菌硝基还原酶(NTR)的荧光探针,并对其性质和生物学应用进行了研究。所选择的荧光探针 3 在被 NTR 催化还原为中间对位取代的氨苯甲基后,会发生重排消除反应,从而产生快速的 10 倍荧光响应。此外,探针 3 可穿透革兰氏阳性和革兰氏阴性细菌的细胞膜,对 NTR 具有选择性,而对其他生物分析物的背景信号最小化,从而能够实时在活细菌细胞内对 NTR 进行成像。