Han Bingyan, Yuan Jipei, Wang Erkang
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Graduate School of the Chinese Academy of Sciences, Changchun, Jilin, 130022, China.
Anal Chem. 2009 Jul 1;81(13):5569-73. doi: 10.1021/ac900769h.
Herein, a sensitive and selective sensor for biothiols based on the recovered fluorescence of the CdTe quantum dots (QDs)-Hg(II) system is reported. Fluorescence of QDs could be quenched greatly by Hg(II). In the presence of biothiols, such as glutathione (GSH), homocysteine (Hcy), and cysteine (Cys), however, Hg(II) preferred to react with them to form the Hg(II)-S bond because of the strong affinity with the thiols of biothiols rather than quenching the fluorescence of the QDs. Thus, the fluorescence of CdTe QDs was recovered. The restoration ability followed the order GSH > Hcy > Cys due to the decreased steric hindrance effect. A good linear relationship was obtained from 0.6 to 20.0 micromol L(-1) for GSH and from 2.0 to 20.0 micromol L(-1) for Cys, respectively. The detection limits of GSH and Cys were 0.1 and 0.6 micromol L(-1), respectively. In addition, the method showed a high selectivity for Cys among the other 19 amino acids. Furthermore, it succeeded in detecting biothiols in the Hela cell.
本文报道了一种基于碲化镉量子点(QDs)-汞(II)体系荧光恢复的生物硫醇灵敏且选择性的传感器。量子点的荧光可被汞(II)显著猝灭。然而,在存在生物硫醇如谷胱甘肽(GSH)、同型半胱氨酸(Hcy)和半胱氨酸(Cys)时,由于汞(II)与生物硫醇的硫醇基具有很强的亲和力,它更倾向于与它们反应形成汞(II)-硫键,而不是猝灭量子点的荧光。因此,碲化镉量子点的荧光得以恢复。由于空间位阻效应降低,恢复能力遵循GSH > Hcy > Cys的顺序。GSH在0.6至20.0微摩尔/升范围内以及Cys在2.0至20.0微摩尔/升范围内分别获得了良好的线性关系。GSH和Cys的检测限分别为0.1和0.6微摩尔/升。此外,该方法在其他19种氨基酸中对Cys表现出高选择性。而且,它成功地检测了HeLa细胞中的生物硫醇。