Enzyme-free and triple-amplified electrochemical sensing of 8-hydroxy-2′-deoxyguanosine by three kinds of short pDNA-driven catalyzed hairpin assemblies followed by a hybridization chain reaction

被引:12
作者
Jia, Li-Ping [1 ]
Feng, Zhe [1 ]
Zhao, Ruo-Nan [1 ]
Ma, Rong-Na [1 ]
Zhang, Wei [1 ]
Shang, Lei [1 ]
Jia, Wen-Li [1 ]
Wang, Huai-Sheng [1 ]
机构
[1] Liaocheng Univ, Dept Chem, Liaocheng 252000, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFORMANCE LIQUID-CHROMATOGRAPHY; HIGHLY SENSITIVE DETECTION; OXIDATIVE STRESS; CAPILLARY-ELECTROPHORESIS; MASS-SPECTROMETRY; HUMAN URINE; DNA; DAMAGE; ASSAY; 8-OXO-7,8-DIHYDRO-2'-DEOXYGUANOSINE;
D O I
10.1039/d0an00233j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive and enzyme-free electrochemical aptasensor was constructed for the sensing of 8-hydroxy-2 '-deoxyguanosine (8-OH-dG). In the process of constructing the aptasensor, triple signal amplification strategies were introduced to enhance the sensitivity. First, every aptamer/pDNA complex immobilized on magnetic beads could release three kinds of pDNAs when 8-OH-dG was introduced, which caused three-fold magnification of the target. Second, the released three kinds of pDNAs initiated catalyzed hairpin assembly between two hairpin DNAs (HP1 and HP2) on a gold electrode. Meanwhile, the three kinds of pDNAs were released again by a strand displacement reaction to obtain the next catalyzed hairpin assembly. Third, the emerging toehold of HP2 further induced a hybridization chain reaction (HCR) between two hairpin DNAs (HP3 and HP4), forming a long double-stranded DNA concatemer on the surface of the electrode. Finally, [Ru(NH3)(6)](3+), an electroactive cation, was adsorbed onto the long dsDNA concatemer by electrostatic interactions and consequently, an electrochemical signal was generated. Under this triple signal amplification, a low detection limit down to 24.34 fM has been obtained for 8-OH-dG determination, which is superior to those of most previously reported methods.
引用
收藏
页码:3605 / 3611
页数:7
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