Xia Shuai, Fang Mingxi, Wang Jianbo, Bi Jianheng, Mazi Wafa, Zhang Yibin, Luck Rudy L, Liu Haiying
Department of Chemistry, Michigan Technological University, 1400 Townsend Drive, Houghton, MI, 49931, United States.
College of Biological Chemical Sciences and Engineering Jiaxing University, Jiaxing, 314001, China.
Sens Actuators B Chem. 2019 Sep 1;294:1-13. doi: 10.1016/j.snb.2019.05.005. Epub 2019 May 4.
Three fluorescent probes have been developed by conjugating three different BODIPY donors to rhodamine and merocyanine acceptors for ratiometric determination of lysosomal pH variations. Probe consists of a 1,3,5,7-tetramethyl-BODIPY donor and a near-infrared rhodamine acceptor bearing a lysosome-targeting morpholine residue. Probe is composed of a 3,5-dimethyl-BODIPY donor and a near-infrared rhodamine acceptor modified with an -phenylenediamine residue. Probe contains a 3-styrene-functionalized BODIPY donor with longer wavelength emission and a near-infrared merocyanine acceptor containing a morpholine residue. Under neutral or basic pH conditions, the probes only show fluorescence from the BODIPY donors under BODIPY excitation because the rhodamine and merocyanine acceptors maintain closed spirolactam configurations. However, excitation at BODIPY absorption wavelengths concomitant with gradual pH decrease results in fluorescence decreases with the BODIPY donors and fluorescence increases from the rhodamine and merocyanine acceptors due to through-bond energy transfer from the donors to the acceptors. This is because the spirolactam ring opens under more acidic conditions and fluorescence of the acceptors results from significantly improved π-conjugation. These experimental results are substantiated with theoretical calculations on models of the different probes. The probes have all been used to determine lysosome pH variations in HeLa cells. Probe was further utilized to successfully detect pH fluctuations in HeLa cells under oxidative stress and with treatment of NHCl and chloroquine.
通过将三种不同的硼二吡咯供体与罗丹明和部花青受体共轭,开发了三种荧光探针,用于比率测定溶酶体pH值变化。探针1由1,3,5,7-四甲基硼二吡咯供体和带有溶酶体靶向吗啉残基的近红外罗丹明受体组成。探针2由3,5-二甲基硼二吡咯供体和用对苯二胺残基修饰的近红外罗丹明受体组成。探针3包含具有更长波长发射的3-苯乙烯官能化硼二吡咯供体和含有吗啉残基的近红外部花青受体。在中性或碱性pH条件下,由于罗丹明和部花青受体保持封闭的螺内酰胺构型,探针在硼二吡咯激发下仅显示来自硼二吡咯供体的荧光。然而,在硼二吡咯吸收波长处激发并伴随pH逐渐降低,会导致硼二吡咯供体的荧光降低,而由于从供体到受体的键间能量转移,罗丹明和部花青受体的荧光增加。这是因为螺内酰胺环在更酸性条件下打开,受体的荧光源于显著改善的π共轭。这些实验结果通过对不同探针模型的理论计算得到证实。这些探针均已用于测定HeLa细胞中的溶酶体pH值变化。探针1还被进一步用于成功检测HeLa细胞在氧化应激以及用NH4Cl和氯喹处理时的pH波动。