Research Center for Analytical Sciences, College of Sciences, Northeastern University, Box 332, Shenyang 110819, China.
Analyst. 2012 Nov 7;137(21):4974-80. doi: 10.1039/c2an36049g. Epub 2012 Sep 12.
A label-free strategy based on the Fenton reaction with DNA-templated silver nanoclusters (DNA-Ag NCs) as a probe is demonstrated for the sequential detection of Cu(2+), ascorbic acid (AA) and H(2)O(2). Cu(2+) causes a structural change of the DNA template in DNA-Ag NCs to resist the environmental quenching and emit stronger fluorescence. The addition of AA in the presence of Cu(2+) results in a further fluorescence increase of the DNA-Ag NCs. Interestingly, an even higher fluorescence enhancement is recorded by introducing Cu(2+) into the DNA-Ag NCs-AA probing system. The fluorescence turn-on probe offers detection limits of 3 nM for Cu(2+) and 7 nM for AA. Thereafter, the addition of H(2)O(2) generates hydroxyl radicals from the Fenton reaction, which induces cleavage of the DNA template, leading to fluorescence quenching of the DNA-Ag NCs. This facilitates H(2)O(2) detection. Moreover, based on the DNA-templated fluorescent silver nanoclusters and Fenton reaction, a multiple logic gate system, including AND and a three-input logic gate, is constructed, with Cu(2+), AA and H(2)O(2) as inputs, and the fluorescence intensity of the DNA-Ag NCs probe as output.
基于 Fenton 反应的无标记策略,利用 DNA 模板银纳米簇(DNA-Ag NCs)作为探针,用于顺序检测 Cu(2+)、抗坏血酸(AA)和 H(2)O(2)。Cu(2+)导致 DNA-Ag NCs 中的 DNA 模板发生结构变化,从而抵抗环境猝灭并发射更强的荧光。在存在 Cu(2+)的情况下加入 AA 会导致 DNA-Ag NCs 的荧光进一步增强。有趣的是,通过将 Cu(2+)引入 DNA-Ag NCs-AA 探测系统,记录到更高的荧光增强。该荧光开启探针对 Cu(2+)的检测限为 3 nM,对 AA 的检测限为 7 nM。此后,Fenton 反应产生的羟基自由基会引发 DNA 模板的断裂,导致 DNA-Ag NCs 的荧光猝灭,从而实现 H(2)O(2)的检测。此外,基于 DNA 模板化荧光银纳米簇和 Fenton 反应,构建了一个多逻辑门系统,包括 AND 和三输入逻辑门,以 Cu(2+)、AA 和 H(2)O(2)作为输入,以 DNA-Ag NCs 探针的荧光强度作为输出。