In Situ Hybridization Chain Reaction Amplification for Universal and Highly Sensitive Electrochemiluminescent Detection of DNA

被引:264
作者
Chen, Ying [1 ]
Xu, Jin [1 ]
Su, Jiao [1 ]
Xiang, Yun [1 ]
Yuan, Ruo [1 ]
Chai, Yaqin [1 ]
机构
[1] Southwest Univ, Key Lab, Minist Educ Luminescence & Real Time Anal, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
ALKANEBISPHOSPHONATE THIN-FILM; ELECTROGENERATED CHEMILUMINESCENCE; NUCLEIC-ACIDS; INSOLUBLE PRODUCT; ELECTROCHEMICAL DETECTION; SIGNAL AMPLIFICATION; HAIRPIN DNA; BIOSENSOR; IMMOBILIZATION; PROBE;
D O I
10.1021/ac3012285
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we describe a new universal and highly sensitive strategy for electrochemiluminescent (ECL) detection of sequence specific DNA at the femtomolar level via in situ hybridization chain reaction (HCR) signal amplification. The DNA capture probes are self-assembled on a gold electrode. The presence of the target DNA and two hairpin helper DNAs leads to the formation of extended dsDNA polymers through HCR on the electrode surface. The in situ, HCR-generated dsDNA polymers cause the intercalation of numerous ECL indicators (Ru(phen)(3)(2+)) into the dsDNA grooves, resulting in significantly amplified ECL signal output. The proposed strategy combines the amplification power of the DNA HCR and the inherent high sensitivity of the ECL technique and enables low femtomolar detection of sequence specific DNA. The developed strategy also shows high selectivity against single-base mismatch sequences, which makes our new universal and highly sensitive HCR-based method a useful addition to the amplified DNA detection arena.
引用
收藏
页码:7750 / 7755
页数:6
相关论文
共 52 条
[31]   Design of electrochemical biosensor systems for the detection of specific DNA sequences in PCR-amplified nucleic acids related to the catechol-O-methyltransferase val1 08/158Met polymorphism based on intrinsic guanine signal [J].
Ozkan-Ariksoysal, Dilsat ;
Tezcanli, Burcin ;
Kosova, Buket ;
Ozsoz, Mehmet .
ANALYTICAL CHEMISTRY, 2008, 80 (03) :588-596
[32]  
Park SJ, 2002, SCIENCE, V295, P1503, DOI 10.1126/science.1067003
[33]   Enzyme-linked amplified electrochemical sensing of oligonucleotide-DNA interactions by means of the precipitation of an insoluble product and using impedance spectroscopy [J].
Patolsky, F ;
Katz, E ;
Bardea, A ;
Willner, I .
LANGMUIR, 1999, 15 (11) :3703-3706
[34]  
Patolsky F, 2002, ANGEW CHEM INT EDIT, V41, P3398, DOI 10.1002/1521-3773(20020916)41:18<3398::AID-ANIE3398>3.0.CO
[35]  
2-W
[36]   Amplified chemiluminescence surface detection of DNA and telomerase activity using catalytic nucleic acid labels [J].
Pavlov, V ;
Xiao, Y ;
Gill, R ;
Dishon, A ;
Kotler, M ;
Willner, I .
ANALYTICAL CHEMISTRY, 2004, 76 (07) :2152-2156
[37]   Examination of Electron Transfer Through DNA Using Electrogene rated Chemiluminescence [J].
Pittman, Tommie Lyndon ;
Miao, Wujian .
JOURNAL OF PHYSICAL CHEMISTRY C, 2008, 112 (43) :16999-17004
[38]   PRIMER-DIRECTED ENZYMATIC AMPLIFICATION OF DNA WITH A THERMOSTABLE DNA-POLYMERASE [J].
SAIKI, RK ;
GELFAND, DH ;
STOFFEL, S ;
SCHARF, SJ ;
HIGUCHI, R ;
HORN, GT ;
MULLIS, KB ;
ERLICH, HA .
SCIENCE, 1988, 239 (4839) :487-491
[39]   Fiber-optic microsphere-based arrays for multiplexed biological warfare agent detection [J].
Song, LN ;
Ahn, S ;
Walt, DR .
ANALYTICAL CHEMISTRY, 2006, 78 (04) :1023-1033
[40]   Detection of point mutation and insertion mutations in DNA using a quartz crystal microbalance and MutS, a mismatch binding protein [J].
Su, XD ;
Robelek, R ;
Wu, YJ ;
Wang, GY ;
Knoll, W .
ANALYTICAL CHEMISTRY, 2004, 76 (02) :489-494