Department of Chemistry, Tongji University, Shanghai 200092, China.
Department of Chemistry, Tongji University, Shanghai 200092, China.
Biosens Bioelectron. 2015 Apr 15;66:103-8. doi: 10.1016/j.bios.2014.11.013. Epub 2014 Nov 11.
In the present study, a new strategy based on Cu(2+) mediated DNA-templated silver nanoclusters (DNA-Ag NCs) was developed, as a label-free, on-off-on fluorescent probe for the detection of l-histidine. Eight synthesized DNA oligonucleotides (D1-D8) were experimentally tested, and D5-Ag NCs was finally selected for l-histidine detection due to its best fluorescent properties. The fluorescence emission of D5-Ag NCs could be quenched by Cu(2+) via electron or energy transfer. Upon addition of l-histidine, the chelation between Cu(2+) and the imidazole group of l-histidine leads to Cu(2+) liberation from D5-Ag NCs, and subsequently results in a dramatic fluorescence enhancement of the probe. The method displayed a good selectivity toward l-histidine over all the other amino acids, with a linear relationship in the range of 0.20-80μM, and a limit of detection (LOD) of 4.3nM. The strategy was also successfully applied to detect l-histidine in diluted human urine, exhibiting great opportunities for practical application in biological system.
在本研究中,开发了一种基于 Cu(2+)介导的 DNA 模板银纳米簇(DNA-Ag NCs)的新策略,作为一种无标记的、开-关-开荧光探针,用于检测 l-组氨酸。实验测试了 8 种合成的 DNA 寡核苷酸(D1-D8),最终选择 D5-Ag NCs 用于 l-组氨酸检测,因为它具有最佳的荧光特性。D5-Ag NCs 的荧光发射可以通过电子或能量转移被 Cu(2+)猝灭。加入 l-组氨酸后,Cu(2+)与 l-组氨酸的咪唑基团之间的螯合作用导致 Cu(2+)从 D5-Ag NCs 中释放出来,从而使探针的荧光显著增强。该方法对 l-组氨酸表现出良好的选择性,相对于所有其他氨基酸,在 0.20-80μM 范围内呈现线性关系,检测限(LOD)为 4.3nM。该策略还成功地应用于检测稀释的人尿中的 l-组氨酸,在生物体系中具有很大的实际应用潜力。