Zhao Ming, Fan Gao-Chao, Chen Jing-Jia, Shi Jian-Jun, Zhu Jun-Jie
School of Chemical Engineering, Anhui University of Science and Technology , Huainan 232001, People's Republic of China.
State Key Laboratory of Analytical Chemistry for Life Science, Collaborative Innovation Center of Chemistry for Life Sciences, School of Chemistry and Chemical Engineering, Nanjing University , Nanjing 210093, People's Republic of China.
Anal Chem. 2015 Dec 15;87(24):12340-7. doi: 10.1021/acs.analchem.5b03721. Epub 2015 Dec 4.
A highly sensitive and selective photoelectrochemical (PEC) biosensor for Hg(2+) detection was developed on the basis of the synergistic effect of exciton energy transfer (EET) between CdS quantum dots (QDs) and Au nanoparticles (NPs) coupled with sensitization of rhodamine 123 (Rh123) for signal amplification. First, the TiO2/CdS hybrid structure obtained by depositing CdS QDs on TiO2 film was employed as a matrix for immobilizing probe DNA (pDNA). Next, Rh123 was introduced into the pDNA terminal, and then Au NP labeled target DNA (Au-tDNA) was hybridized with pDNA to form a rod-like double helix structure. The detection of Hg(2+) was based on a conformational change of the pDNA after incubating with Hg(2+). In the absence of Hg(2+), Rh123 was located away from the electrode surface due to the DNA hybridization, leading to inhibition of the sensitization effect, and meanwhile, the occurrence of EET between CdS QDs and Au NPs resulted in a photocurrent decrease. However, after incubating with Hg(2+), the rod-like double helix was disrupted, and the energy transfer was broken. In this case, the photocurrent recovered, and meanwhile, the folded pDNA made the labeled Rh123 move closer to the electrode surface, leading to the formation of the sensitization structure, which evidently increased the photocurrent intensity. The sensitivity of the biosensor for Hg(2+) detection was greatly enhanced for the dual signal amplification strategy. The linear range was 10 fM to 200 nM, with a detection limit of 3.3 fM. This biosensor provides a promising new platform for detecting various heavy metal ions at ultralow levels.
基于硫化镉(CdS)量子点(QDs)与金纳米颗粒(NPs)之间的激子能量转移(EET)协同效应,并结合罗丹明123(Rh123)的敏化作用以实现信号放大,开发了一种用于检测Hg(2+)的高灵敏度和高选择性光电化学(PEC)生物传感器。首先,通过在TiO2薄膜上沉积CdS量子点获得的TiO2/CdS杂化结构被用作固定探针DNA(pDNA)的基质。接下来,将Rh123引入pDNA末端,然后将金纳米颗粒标记的靶DNA(Au-tDNA)与pDNA杂交形成棒状双螺旋结构。Hg(2+)的检测基于pDNA与Hg(2+)孵育后的构象变化。在没有Hg(2+)的情况下,由于DNA杂交,Rh123远离电极表面,导致敏化效应受到抑制,同时,CdS量子点与金纳米颗粒之间发生EET导致光电流降低。然而,与Hg(2+)孵育后,棒状双螺旋被破坏,能量转移中断。在这种情况下,光电流恢复,同时,折叠的pDNA使标记的Rh123更靠近电极表面,导致敏化结构的形成,这明显增加了光电流强度。由于采用了双信号放大策略,该生物传感器对Hg(2+)检测的灵敏度大大提高。线性范围为10 fM至200 nM,检测限为3.3 fM。这种生物传感器为超痕量检测各种重金属离子提供了一个有前景的新平台。