Gao Min, Wang Rui, Yu Fabiao, You Jinmao, Chen Lingxin
The Key Laboratory of Life-Organic Analysis, College of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, China.
Analyst. 2015 Jun 7;140(11):3766-72. doi: 10.1039/c4an02366h.
Hydrogen polysulfides (H2Sn, n > 1), derived from hydrogen sulfide (H2S), have been considered to be involved in cytoprotective processes and redox signaling. The emerging evidences imply that the actual signaling molecule is H2Sn rather than H2S. In this work, we present a near-infrared fluorescent probe BD-ss for the selective detection of H2Sn biosynthetic pathways in living cells and in vivo. The probe is constructed by equipping a bis-electrophilic H2Sn capture group p-nitrofluorobenzoate to a near-infrared fluorophore azo-BODIPY. BD-ss can provide a remarkable turn-on fluorescence response for assessing endogenous H2Sn formation ways in serum, in living cells and in vivo.
多硫化氢(H2Sn,n>1)由硫化氢(H2S)衍生而来,被认为参与细胞保护过程和氧化还原信号传导。新出现的证据表明,实际的信号分子是H2Sn而非H2S。在这项工作中,我们提出了一种近红外荧光探针BD-ss,用于选择性检测活细胞和体内的H2Sn生物合成途径。该探针是通过将双亲电H2Sn捕获基团对硝基氟苯甲酸酯与近红外荧光团偶氮-硼二吡咯相结合构建而成。BD-ss能够提供显著的荧光开启响应,用于评估血清、活细胞和体内内源性H2Sn的形成方式。