Electrochemical Aptameric Recognition System for a Sensitive Protein Assay Based on Specific Target Binding-Induced Rolling Circle Amplification

被引:109
作者
Wu, Zai-Sheng [1 ]
Zhou, Hui [1 ]
Zhang, Songbai [1 ]
Shen, Guoli [1 ]
Yu, Ruqin [1 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
LABEL-FREE; DNA APTAMERS; SIGNALING APTAMERS; BIOLOGICAL-FLUIDS; AU NANOPARTICLES; CATALYTIC LABELS; METHYLENE-BLUE; GROWTH-FACTOR; BIOSENSOR; SENSORS;
D O I
10.1021/ac902400n
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A reusable aptameric recognition system was described for the electrochemical detection of the protein PDGF-BB based on the target binding-induced rolling circle amplification (RCA). A complementary DNA (CDNA), linear padlock probe, and primer probe were utilized to introduce a RCA process into the aptamer-target binding event while a new aptamer was elegantly designed via lengthening the original aptamer by the complement to the CDNA. The aptameric sensing system facilitates the integration of multiple functional elements into a signaling scheme: a unique electrochemical technique, an attractive RCA process, reversible DNA hybridization, and desirable aptameric target recognition. This RCA-based electrochemical recognition system not only exhibits excellent performance (e.g., a detection limit of 6.3 x 10(-11) M, a linear dynamic range of 2 orders of magnitude, high specificity, and satisfactory repeatability) but also overcomes the limitations associated with conventional aptameric biosensors (e.g., dependence of signaling target binding on specific aptamer sequence or requirement of sandwich assays for two or more binding sites per target molecule). A recovery test demonstrated the feasibility of the developed target protein assay. Given the attractive characteristics, this aptameric recognition platform is expected to be a candidate for the detection of proteins and other ligands of interest in both fundamental and applied research.
引用
收藏
页码:2282 / 2289
页数:8
相关论文
共 57 条
[1]  
Baker BR, 2006, J AM CHEM SOC, V128, P3138, DOI 10.1021/ja056957p
[2]   Using a deoxyribozyme ligase and rolling circle amplification to detect a non-nucleic acid analyte, ATP [J].
Cho, EJ ;
Yang, LT ;
Levy, M ;
Ellington, AD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (07) :2022-2023
[3]   Proximity extension of circular DNA aptamers with real-time protein detection [J].
Di Giusto, DA ;
Wlassoff, WA ;
Gooding, JJ ;
Messerle, BA ;
King, GC .
NUCLEIC ACIDS RESEARCH, 2005, 33 (06) :1-7
[4]   Multifunctional label-free electrochemical biosensor based on an integrated aptamer [J].
Du, Yan ;
Li, Bingling ;
Wei, Hui ;
Wang, Yuling ;
Wang, Erkang .
ANALYTICAL CHEMISTRY, 2008, 80 (13) :5110-5117
[5]   Functional aptamers and aptazymes in biotechnology, diagnostics, and therapy [J].
Famulok, Michael ;
Hartig, Jorg S. ;
Mayer, Gunter .
CHEMICAL REVIEWS, 2007, 107 (09) :3715-3743
[6]   Synthetic DNA aptamers to detect protein molecular variants in a high-throughput fluorescence quenching assay [J].
Fang, XH ;
Sen, A ;
Vicens, M ;
Tan, WH .
CHEMBIOCHEM, 2003, 4 (09) :829-834
[7]   Label-free electrochemical detection of nanomolar adenosine based on target-induced aptamer displacement [J].
Feng, Kejun ;
Sun, Chenhu ;
Kang, Yan ;
Chen, Jiwei ;
Jiang, Jian-Hui ;
Shen, Guo-Li ;
Yu, Ru-Qin .
ELECTROCHEMISTRY COMMUNICATIONS, 2008, 10 (04) :531-535
[8]   Protein detection via direct enzymatic amplification of short DNA aptamers [J].
Fischer, Nicholas O. ;
Tarasow, Theodore M. ;
Tok, Jeffrey B. -H. .
ANALYTICAL BIOCHEMISTRY, 2008, 373 (01) :121-128
[9]   Protein detection using proximity-dependent DNA ligation assays [J].
Fredriksson, S ;
Gullberg, M ;
Jarvius, J ;
Olsson, C ;
Pietras, K ;
Gústafsdóttir, SM ;
Östman, A ;
Landegren, U .
NATURE BIOTECHNOLOGY, 2002, 20 (05) :473-477
[10]   Pt nanopartictes functionalized with nucleic acid act as catalytic labels for the chemiluminescent detection of DNA and proteins [J].
Gill, Ron ;
Polsky, Ronen ;
Willner, Itamar .
SMALL, 2006, 2 (8-9) :1037-1041