Citation: ZHANG He, WANG Qing, FU Xin, ZHAO Zhi-Liang. Fabrication of “Turn-On” Sensor for Sensitive Detection of Hg2+ Based on Rolling Circle Amplification and Tandem G-quadruplex-hemin DNAzymes[J]. Chinese Journal of Analytical Chemistry, ;2018, 46(10): 1644-1651. doi: 10.11895/j.issn.0253-3820.181346
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Based on the tandem G-quadruplex-hemin DNAzymes for catalytic signal amplification and T-Hg2+-T structure for specific recognition, a highly sensitive "Turn-on" biosensor for detection of mercury ion (Hg2+) was developed on the polystyrene microbeads to achieve the detection of Hg2+ in urine samples. Through the specific binding of streptavidin and biotin, the T-rich biotinylated Hg2+ capture probe was immobilized on the surface of the microspheres. When Hg2+ was present in reaction system, the T-rich Hg2+ capture probe could capture the cyclic DNA containing G-quadruplex complementary fragments to the surface of beads by forming T-Hg2+-T structure. Through rolling circle amplification, a large number of tandem G-quadruplex forming sequences were amplified. When hemin was inserted into the G-quadruplex, a G-quadruplex-hemin DNAzyme with enhanced catalytic activity was formed, which could catalyze the oxidation of ABTS to ABTS·+ under the condition of H2O2. Finally, the absorbance difference at 420 nm was detected by UV-vis spectrophotometer. Under the optimal experimental conditions, the linear range for detection of Hg2+ was 0.4 pmol/L-100 pmol/L with the detection limit of 0.3 pmol/L, and the regression equation was ΔA420 nm=0.1+0.0019CHg2+ (pmol/L). This Hg2+ sensing system had excellent selectivity for Hg2+ against other possible competing ions. The fabricated sensor was applied to detection of Hg2+ in urine samples, the relative standard deviation and the recovery were 1.4%-2.6% and 94.0%-106.0%, respectively. The sensor had good selectivity, sensitivity, anti-interference ability and reliable detection capability for complex practical samples.
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