Li Chao, Wei Luming, Liu Xinjian, Lei Lin, Li Genxi
Department of Biochemistry and State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing 210093, PR China.
Department of Biochemistry and State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing 210093, PR China; Laboratory of Biosensing Technology, School of Life Sciences, Shanghai University, Shanghai 200444, PR China.
Anal Chim Acta. 2014 Jun 11;831:60-4. doi: 10.1016/j.aca.2014.05.001. Epub 2014 May 2.
In this paper, we report a novel colorimetric strategy for the detection of small molecules by using Pb(2+) ion as an example. In this strategy, DNAzyme duplex modified gold nanoparticles (GNPs) are designed to be unable to interact with graphene oxide (GO). However, in the presence of Pb(2+), the substrate strand of the DNAzyme is cleaved at its cleavage site, resulting in the disassembly of the DNAzyme duplex modified GNPs into three parts, i.e., the 3'- and 5'-fragments of substrate strand and the DNAzyme strand modified GNPs. By taking advantage of the efficient cross-linking effect of ssDNA-GNPs to GO, colorimetric sensor for the detection of the metal ion can be fabricated with a detection limit of 100 pM, which is much lower than the previous reports. This colorimetric method has also been used for the determination of Pb(2+) in the tap water of the local city and the water from a reservoir with satisfactory results, so it may have potential applications in the future.
在本文中,我们以Pb(2+)离子为例,报道了一种用于检测小分子的新型比色策略。在该策略中,设计了DNAzyme双链修饰的金纳米颗粒(GNPs)使其无法与氧化石墨烯(GO)相互作用。然而,在Pb(2+)存在的情况下,DNAzyme的底物链在其切割位点被切割,导致DNAzyme双链修饰的GNPs分解为三部分,即底物链的3'-和5'-片段以及DNAzyme链修饰的GNPs。利用单链DNA-GNPs对GO的高效交联作用,可制备用于检测金属离子的比色传感器,其检测限为100 pM,远低于先前的报道。这种比色方法还用于测定当地城市的自来水和水库水中的Pb(2+),结果令人满意,因此它在未来可能具有潜在的应用。