Department of Chemistry, SRM University, Kattankulathur, 603 203, Chennai, India.
Environmental Technology Division, School of Industrial Technology, University Sains Malaysia, 11800, Minden, Penang, Malaysia.
J Fluoresc. 2017 Nov;27(6):2101-2109. doi: 10.1007/s10895-017-2149-4. Epub 2017 Aug 17.
A label -free DNAzyme amplified biosensor is found to be highly selective and sensitive towards fluorescent detection of Pb ions in aqueous media. The DNAzyme complex has designed by the hybridization of the enzyme and substrate strand. In the presence of Pb, the DNAzyme activated and cleaved the substrate strand of RNA site (rA) into two oligonucleotide fragments. Further, the free fragment was hybridized with a complementary strand on the surface of MBs. After magnetic separation, SYBER Green I was added and readily intercalate with the dsDNA to gives a bright fluorescence signal with intensity directly proportional to the concentration of Pbions. A detection limit of 5 nM in Pb the detection range 0 to 500 nM was obtained. This label- free fluorescent biosensor has been successfully applied to the determination of environmental water samples. Then results open up the possibility for real-time quantitative detection of Pb with convenient potential applications in the biological and environmental field. Graphical Abstract.
无标记 DNAzyme 放大生物传感器被发现对水溶液中 Pb 离子的荧光检测具有高度选择性和灵敏度。DNAzyme 复合物是通过酶和底物链的杂交设计的。在 Pb 存在下,DNAzyme 被激活并将 RNA 位点(rA)的底物链切割成两个寡核苷酸片段。进一步地,游离片段与 MBs 表面的互补链杂交。磁分离后,加入 SYBER Green I,它很容易与 dsDNA 嵌入,给出与 Pb 离子浓度成正比的强荧光信号。在 Pb 的检测范围内(0 到 500 nM),检测限为 5 nM。该无标记荧光生物传感器已成功应用于环境水样的测定。这些结果为实时定量检测 Pb 开辟了可能性,具有在生物和环境领域的潜在应用。