Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry and Materials Science, Shaanxi Normal University, Xi'an 710062, PR China.
Anal Chim Acta. 2011 Jan 10;683(2):234-41. doi: 10.1016/j.aca.2010.10.030. Epub 2010 Oct 30.
A highly reproducible and sensitive signal-on electrogenerated chemiluminescence (ECL) biosensor based on the DNAzyme for the determination of lead ion was developed. The ECL biosensor was fabricated by covalently coupling 5'-amino-DNAzyme-tagged with ruthenium bis (2,2'-bipyridine) (2,2'-bipyridine-4,4'-dicarboxylic acid)-ethylenediamine (Ru1-17E') onto the surface of graphite electrode modified with 4-aminobenzoic acid, and then a DNA substrate with a ribonucleotide adenosine hybridized with Ru1-17E' on the electrode. Upon binding of Pb(2+) to the Ru1-17E' to form a complex which catalyzed the cleavage of the DNA substrate, the double-stranded DNA was dissociated and thus led to a high ECL signal. The signal linearly increases with the concentration of Pb(2+) in the range from 5.0 to 80 pM with a detection limit of 1.4 pM and a relative standard derivation of 2.3%. This work demonstrates that using DNAzyme tagged with ruthenium complex as an ECL probe and covalently coupling method for the fabrication of the ECL biosensor with high sensitivity, good stability and significant regeneration ability is promising approach.
基于 DNA 酶的高重现性和高灵敏度电致化学发光(ECL)生物传感器用于测定铅离子。该 ECL 生物传感器通过将 5'-氨基-DNA 酶标记的钌双(2,2'-联吡啶)(2,2'-联吡啶-4,4'-二羧酸)-乙二胺(Ru1-17E')共价偶联到 4-氨基苯甲酸修饰的石墨电极表面上而制备,然后将带有与 Ru1-17E'杂交的核苷酸腺苷的 DNA 底物固定在电极上。当 Pb(2+)与 Ru1-17E'结合形成一种可以催化 DNA 底物切割的复合物时,双链 DNA 会解离,从而导致 ECL 信号增强。该信号与 Pb(2+)的浓度在 5.0 至 80 pM 范围内呈线性增加,检测限为 1.4 pM,相对标准偏差为 2.3%。这项工作表明,使用标记有钌复合物的 DNA 酶作为 ECL 探针,以及通过共价偶联方法制备 ECL 生物传感器具有高灵敏度、良好的稳定性和显著的再生能力,是一种很有前途的方法。