Rational, modular adaptation of enzyme-free DNA circuits to multiple detection methods

被引:443
作者
Li, Bingling [1 ]
Ellington, Andrew D. [1 ]
Chen, Xi [1 ]
机构
[1] Univ Texas Austin, Inst Cellular & Mol Biol, Ctr Syst & Synthet Biol, Dept Chem & Biochem, Austin, TX 78712 USA
关键词
ROLLING CIRCLE AMPLIFICATION; CLEAVING DEOXYRIBOZYME; PROXIMITY LIGATION; BRANCH MIGRATION; IMMUNO-PCR; RNA; NANOTECHNOLOGY; SENSITIVITY; EXPRESSION; BIOSENSOR;
D O I
10.1093/nar/gkr504
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Signal amplification is a key component of molecular detection. Enzyme-free signal amplification is especially appealing for the development of low-cost, point-of-care diagnostics. It has been previously shown that enzyme-free DNA circuits with signal-amplification capacity can be designed using a mechanism called 'catalyzed hairpin assembly'. However, it is unclear whether the efficiency and modularity of such circuits is suitable for multiple analytical applications. We have therefore designed and characterized a simplified DNA circuit based on catalyzed hairpin assembly, and applied it to multiple different analytical formats, including fluorescent, colorimetric, and electrochemical and signaling. By optimizing the design of previous hairpin-based catalytic assemblies we found that our circuit has almost zero background and a high catalytic efficiency, with a k(cat) value above 1 min(-1). The inherent modularity of the circuit allowed us to readily adapt our circuit to detect both RNA and small molecule analytes. Overall, these data demonstrate that catalyzed hairpin assembly is suitable for analyte detection and signal amplification in a 'plug-and-play' fashion.
引用
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页数:13
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共 60 条
[1]
Sensitivity by combination: immuno-PCR and related technologies [J].
Adler, Michael ;
Wacker, Ron ;
Niemeyer, Christof M. .
ANALYST, 2008, 133 (06) :702-718
[2]
An autonomous molecular computer for logical control of gene expression [J].
Benenson, Y ;
Gil, B ;
Ben-Dor, U ;
Adar, R ;
Shapiro, E .
NATURE, 2004, 429 (6990) :423-429
[3]
Kinetic and thermodynamic characterization of the RNA-cleaving 8-17 deoxyribozyme [J].
Bonaccio, M ;
Credali, A ;
Peracchi, A .
NUCLEIC ACIDS RESEARCH, 2004, 32 (03) :916-925
[4]
A DNA ENZYME WITH MG2+-DEPENDENT RNA PHOSPHOESTERASE ACTIVITY [J].
BREAKER, RR ;
JOYCE, GF .
CHEMISTRY & BIOLOGY, 1995, 2 (10) :655-660
[5]
Allosteric hammerhead ribozyme TRAPs [J].
Burke, DH ;
Ozerova, NDS ;
Nilsen-Hamilton, M .
BIOCHEMISTRY, 2002, 41 (21) :6588-6594
[6]
Ultrasensitive detection of DNA by the PCR-induced generation of DNAzymes: The DNAzyme primer approach [J].
Cheglakov, Zoya ;
Weizmann, Yossi ;
Beissenhirtz, Moritz K. ;
Willner, Itamar .
CHEMICAL COMMUNICATIONS, 2006, (30) :3205-3207
[7]
Construction of molecular logic gates with a DNA-cleaving deoxyribozyme [J].
Chen, X ;
Wang, YF ;
Liu, Q ;
Zhang, ZZ ;
Fan, CH ;
He, L .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (11) :1759-1762
[8]
Design Principles for Ligand-Sensing, Conformation-Switching Ribozymes [J].
Chen, Xi ;
Ellington, Andrew D. .
PLOS COMPUTATIONAL BIOLOGY, 2009, 5 (12)
[9]
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
[10]
Programmable in situ amplification for multiplexed imaging of mRNA expression [J].
Choi, Harry M. T. ;
Chang, Joann Y. ;
Trinh, Le A. ;
Padilla, Jennifer E. ;
Fraser, Scott E. ;
Pierce, Niles A. .
NATURE BIOTECHNOLOGY, 2010, 28 (11) :1208-U103