Department of Chemistry, Dongguk University , Seoul 04620, Republic of Korea.
Division of Curriculum and Textbook, Korea Institute for Curriculum and Evaluation , Seoul 04518, Republic of Korea.
Anal Chem. 2016 Jul 19;88(14):7178-82. doi: 10.1021/acs.analchem.6b01346. Epub 2016 Jul 1.
We report a chromogenic and fluorescence turn-on probe based on crotonoyl ester-functionalized oxazolidinoindole for the selective detection of cysteine in neutral buffer. The probe rapidly formed indocyanophenolate through the Michael addition and a subsequent cyclization reaction of cysteine, inducing both a dramatic bathochromic shift (>130 nm) and a large fluorescence turn-on response (F/F0 12) in the UV-vis and fluorescence spectra and affording a micromolar limit of detection (LOD = 5.0 μM) of cysteine in HEPES buffer. When cysteine was added, the probe exhibited a dual optical change with strong green fluorescence and dramatic red color by the oxazolidinoindole-to-hydroxyethylindolium transformation. Further cellular application of the probe was successfully performed for the mitochondrial imaging of HeLa cells.
我们报告了一种基于巴豆酰酯功能化恶唑烷并吲哚的比色和荧光开启探针,用于在中性缓冲液中选择性检测半胱氨酸。探针通过半胱氨酸的迈克尔加成和随后的环化反应迅速形成靛氰酚盐,在紫外可见和荧光光谱中引起明显的红移 (>130nm)和大的荧光开启响应(F/F0 12),在 HEPES 缓冲液中对半胱氨酸的检测限(LOD=5.0μM)达到微摩尔级。当加入半胱氨酸时,探针通过恶唑烷并吲哚到羟乙基吲哚鎓的转化表现出双重光学变化,具有强绿色荧光和显著的红色。进一步将探针成功应用于 HeLa 细胞的线粒体成像。