Xu Xiaowen, Wang Juan, Jiao Kui, Yang Xiurong
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, Jilin, China.
Biosens Bioelectron. 2009 Jun 15;24(10):3153-8. doi: 10.1016/j.bios.2009.03.025. Epub 2009 Mar 25.
Here, we report a simple and sensitive colorimetric detection method for Hg(2+) ions with a tunable detection range based on DNA oligonucleotides and unmodified gold nanoparticles (DNA/AuNPs) sensing system. Complementary DNA strands with T-T mismatches could effectively protect AuNPs from salt-induced aggregation. While in the presence of Hg(2+) ions T-Hg(2+)-T coordination chemistry leads to the formation of DNA duplexes, and AuNPs are less well protected thus aggregate at the same salt concentration, accompanying by color change from red to blue. By rationally varying the number of T-T mismatches in DNA oligonucleotides, the detection range could be tuned. Employing duplex oligonucleotides with 4 T-T mismatches in the sensing system, a sensitive linear range for Hg(2+) ions from 0 to 5 microM and a detection limit of 0.5 microM are obtained. Adding the number of T-T mismatches to 6 and 8, the assay region is enlarged and linear range is tuned. A low proportion of T-T mismatches makes the detection range narrow but the sensitivity high while a high proportion influences the detection limit but enlarges assay region. Besides, the sensor also shows a good selectivity for Hg(2+).
在此,我们报道了一种基于DNA寡核苷酸和未修饰金纳米颗粒(DNA/AuNPs)传感系统的简单且灵敏的Hg(2+)离子比色检测方法,其检测范围可调。带有T-T错配的互补DNA链能够有效保护金纳米颗粒免受盐诱导的聚集。而在Hg(2+)离子存在的情况下,T-Hg(2+)-T配位化学导致DNA双链体的形成,并且在相同盐浓度下金纳米颗粒受到的保护较少,从而发生聚集,同时伴随着颜色从红色变为蓝色。通过合理改变DNA寡核苷酸中T-T错配的数量,可以调节检测范围。在传感系统中使用具有4个T-T错配的双链寡核苷酸,获得了Hg(2+)离子从0到5 microM的灵敏线性范围以及0.5 microM的检测限。将T-T错配的数量增加到6和8时,检测区域扩大且线性范围得到调节。低比例的T-T错配使检测范围变窄但灵敏度高,而高比例则影响检测限但扩大检测区域。此外,该传感器对Hg(2+)还表现出良好的选择性。