Department of Chemistry, Hankuk University of Foreign Studies , Yongin 449-791, Republic of Korea.
J Am Chem Soc. 2014 May 14;136(19):7018-25. doi: 10.1021/ja500962u. Epub 2014 May 1.
Although a lot of mitochondria-targeting biothiol probes have been developed and applied to cellular imaging through thiol-induced disulfide cleavage or Michael addition reactions, relatively few probes assess mitochondrial GSH with high selectivity over Cys and Hcy and with NIR fluorescence capable of noninvasive imaging in biological samples. In order to monitor mitochondrial GSH with low background autofluorescence, we designed a heptamethine-azo conjugate as an NIR fluorescent probe by introducing a tunable lipophilic cation unit as the biomarker for mitochondria and a nitroazo group as the GSH-selective reaction site as well as the fluorescence quencher. The probe exhibited a dramatic off-on NIR fluorescence response toward GSH with high selectivity over other amino acids including Cys and Hcy. Further application to cellular imaging indicated that the probe was highly responsive to the changes of mitochondrial GSH in cells.
虽然已经开发出许多靶向线粒体的生物硫醇探针,并通过巯基诱导的二硫键断裂或迈克尔加成反应应用于细胞成像,但只有相对较少的探针能够高选择性地评估线粒体 GSH 与半胱氨酸和高半胱氨酸的比值,并且具有近红外(NIR)荧光,能够在生物样本中进行非侵入性成像。为了监测线粒体 GSH 的低背景自发荧光,我们设计了一种七甲川-偶氮缀合物作为近红外荧光探针,通过引入可调脂阳离子单元作为线粒体的生物标志物,以及硝基偶氮基团作为 GSH 选择性反应位点和荧光猝灭剂。该探针对 GSH 表现出显著的近红外荧光开/关响应,对包括半胱氨酸和高半胱氨酸在内的其他氨基酸具有高选择性。进一步应用于细胞成像表明,该探针对细胞中线粒体 GSH 的变化高度敏感。