Xu Jiacui, Sun Yanhong, Sheng Yongjie, Fei Yanqun, Zhang Jin, Jiang Dazhi
Key Laboratory for Molecular Enzymology and Engineering of the Ministry of Education, College of Life Science, Jilin University, Qianjin Street 2699, 130012, Changchun, China.
Anal Bioanal Chem. 2014 May;406(13):3025-9. doi: 10.1007/s00216-014-7732-9. Epub 2014 Mar 28.
The development of a simple sensor (9NL27-Zn) based on DNAzyme and PCR and aimed at the detection of low concentrations of zinc (II) ions is described. A specific Zn(II)-dependent DNAzyme (9NL27) with DNA-cleaving activity was employed. In the presence of zinc (II), the DNAzyme hydrolyzed DNA substrate into two pieces (5' and 3' fragments), forming 3'-terminal hydroxyl in the 5' fragment and 5'-phosphate in the 3' fragments. Subsequently, the 5' fragment left the DNAzyme and bound a short DNA template. The 5' fragment was used as a primer and extended a single-stranded full-length template by Taq polymerase. Finally, this full-length template was amplified by PCR. The amplified products had a quantitative relationship with Zn(II) concentration. Under our experimental conditions, the DNA sensor showed sensitivity (10 nM) and high specificity for zinc ion detection. After improvement of the DNA sensor, the detection limit can reach 1 nM. The simple DNA sensor may become a DNA model for the detection of trace amounts of other targets.
本文描述了一种基于DNAzyme和PCR的简单传感器(9NL27-Zn)的开发,该传感器旨在检测低浓度的锌(II)离子。使用了具有DNA切割活性的特定锌(II)依赖性DNAzyme(9NL27)。在锌(II)存在的情况下,DNAzyme将DNA底物水解成两段(5'和3'片段),在5'片段中形成3'-末端羟基,在3'片段中形成5'-磷酸。随后,5'片段离开DNAzyme并与短DNA模板结合。5'片段用作引物,并通过Taq聚合酶延伸单链全长模板。最后,通过PCR扩增该全长模板。扩增产物与锌(II)浓度具有定量关系。在我们的实验条件下,该DNA传感器对锌离子检测显示出灵敏度(10 nM)和高特异性。经过DNA传感器的改进,检测限可达到1 nM。这种简单的DNA传感器可能成为检测痕量其他目标的DNA模型。