College of Tobacco Science, Henan Agricultural University, Zhengzhou, 450002, P. R. China.
School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.
Sci Rep. 2018 Aug 13;8(1):12021. doi: 10.1038/s41598-018-30529-z.
A novel turn-off colorimetric sensor for sequence-specific recognition of single-stranded DNA (ssDNA) was established by combining Y-shaped DNA duplex and G-quadruplex-hemin DNAzyme. A G-rich single-stranded DNA (Oligo-1) displays peroxidase mimicking catalytic activity due to the specific binding with hemin in the presence of K, which was able to catalyze the oxidation of colorless 2,2'-azinobis(3-ethylbenzothiazoline)-6-sulfonic acid (ABTS) by HO to generate green ABTS• radical for colorimetric assay. Oligonucleotide 2 (Oligo-2) was partly complementary with Oligo-1 and the target DNA. Upon addition of target DNA, Oligo-1, Oligo-2 and target DNA can hybridize with each other to form Y-shaped DNA duplex. The DNAzyme sequence of Oligo-1 was partly caged into Y-shaped DNA duplex, resulting in the inactivation of the DNAzyme and a sharp decrease of the absorbance of the oxidation product of ABTS. Under the optimum condition, the absorbance decreased linearly with the concentration of target DNA over the range of 1.0-250 nM and the detection limit was 0.95 nM (3σ/slope) Moreover, satisfied result was obtained for the discrimination of single-base or two-base mismatched DNA.
一种用于单链 DNA(ssDNA)序列特异性识别的新型关闭比色传感器通过结合 Y 型 DNA 双链体和 G-四链体-血红素 DNA 酶建立。由于在 K 的存在下与血红素的特异性结合,富含 G 的单链 DNA(寡核苷酸 1)显示出过氧化物酶模拟催化活性,其能够通过 HO 催化无色 2,2'-联氮双(3-乙基苯并噻唑啉)-6-磺酸(ABTS)的氧化,用于比色测定生成绿色 ABTS•自由基。寡核苷酸 2(寡核苷酸 2)与寡核苷酸 1 和靶 DNA 部分互补。加入靶 DNA 后,寡核苷酸 1、寡核苷酸 2 和靶 DNA 可以相互杂交形成 Y 型 DNA 双链体。寡核苷酸 1 的 DNA 酶序列部分被笼入 Y 型 DNA 双链体中,导致 DNA 酶失活,ABTS 的氧化产物的吸光度急剧下降。在最佳条件下,吸光度随靶 DNA 浓度在 1.0-250 nM 范围内呈线性下降,检测限为 0.95 nM(3σ/斜率)。此外,还对单碱基或双碱基错配 DNA 的区分获得了令人满意的结果。