Intelligent DNA machine for the ultrasensitive colorimetric detection of nucleic acids

被引:25
作者
Xu, Jianguo [1 ,2 ]
Qian, Jun [1 ,2 ]
Li, Hongling [1 ,2 ]
Wu, Zai-Sheng [1 ,2 ,3 ]
Shen, Weiyu [1 ,2 ]
Jia, Lee [1 ,2 ]
机构
[1] Fuzhou Univ, Coll Chem, Canc Metastasis Alert & Prevent Ctr, Fuzhou 350002, Peoples R China
[2] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Pharmaceut Photocatalysis, Fuzhou 350002, Peoples R China
[3] 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
Intelligent DNA nanomachine; Cyclical nucleic acid strand-displacement polymerization (CNDP); P53; gene; BIFUNCTIONAL OLIGONUCLEOTIDE PROBE; SURFACE-PLASMON RESONANCE; CHAIN-REACTION ASSAY; LABEL-FREE; ELECTROCHEMICAL DETECTION; FLUORESCENCE DETECTION; P53; AMPLIFICATION; DNAZYME; QUADRUPLEX;
D O I
10.1016/j.bios.2015.08.015
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
As DNA is employed to serve as a smart building block, an increasing interest has been devoted to the development of different DNA-based machines for the specific purpose, for example, the exploration of inter- or intramolecular interaction. In the current contribution, we developed an intelligent DNA machine and its operation can be designed to execute the ultrasensitive calorimetric detection of target nucleic acids. The DNA machine consists of a hairpin probe (HP) and an assistant template (AT). Using p53 gene as the target model to trigger the molecular machine operation, cyclic nucleic acid strand displacement polymerization (CNDP) was specifically induced, leading to the DNAzyme mediated catalytic reaction for signal readout. Specifically, with the help of polymerase and nickase, one target molecule was able to drive DNA nano-mechanical devices one-by-one through the hybridization/polymerization displacement cycles, and every initiated machine continued to operate, causing the dramatic accumulation of G-quadruplex-contained products. The G-quadruplex structure after binding to hemin could act as a horseradish peroxidase (HRP)-mimicking DNAzyme and catalyzed the oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) by H2O2. As a result, an enhanced color change could be detected because of the generation of oxidation product ABTS(circle)(+). In this way, the DNA machine has no any signal loss and enables the quantitative measurement of p53 DNA with a detection limit of 10 fM, indicating great promise for unique application in biomedical research and early clinical diagnosis. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:41 / 47
页数:7
相关论文
共 52 条
[1]   Multisite Analytic Performance Studies of a Real-Time Polymerase Chain Reaction Assay for the Detection of BRAF V600E Mutations in Formalin-Fixed, Paraffin-Embedded Tissue Specimens of Malignant Melanoma [J].
Anderson, Steven ;
Bloom, Kenneth J. ;
Vallera, Dino U. ;
Rueschoff, Josef ;
Meldrum, Cliff ;
Schilling, Robert ;
Kovach, Barbara ;
Lee, Ju Ruey-Jiuan ;
Ochoa, Pam ;
Langland, Rachel ;
Halait, Harkanwal ;
Lawrence, H. Jeffrey ;
Dugan, Michael C. .
ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2012, 136 (11) :1385-1391
[2]   Target-induced self-assembly of DNA nanomachine on magnetic particle for multi-amplified biosensing of nucleic acid, protein, and cancer cell [J].
Bi, Sai ;
Cui, Yangyang ;
Dong, Ying ;
Zhang, Ningbo .
BIOSENSORS & BIOELECTRONICS, 2014, 53 :207-213
[3]   Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound [J].
Bykov, VJN ;
Issaeva, N ;
Shilov, A ;
Hultcrantz, M ;
Pugacheva, E ;
Chumakov, P ;
Bergman, J ;
Wiman, KG ;
Selivanova, G .
NATURE MEDICINE, 2002, 8 (03) :282-288
[4]   Detection of methicillin-resistant Staphylococcus aureus using a gold nanoparticle-based colourimetric polymerase chain reaction assay [J].
Chan, Wai-Sing ;
Tang, Bone S. F. ;
Boost, Maureen V. ;
Chow, Chit ;
Leung, Polly H. M. .
BIOSENSORS & BIOELECTRONICS, 2014, 53 :105-111
[5]   Hairpin assembly-triggered cyclic activation of a DNA machine for label-free and ultrasensitive chemiluminescence detection of DNA [J].
Chen, Jia ;
Qiu, Hongdeng ;
Zhang, Mingliang ;
Gu, Tongnian ;
Shao, Shijun ;
Huang, Yong ;
Zhao, Shulin .
BIOSENSORS & BIOELECTRONICS, 2015, 68 :550-555
[6]   A Comparison of the Cytotoxicity and Proinflammatory Cytokine Production of EndoSequence Root Repair Material and ProRoot Mineral Trioxide Aggregate in Human Osteoblast Cell Culture Using Reverse-Transcriptase Polymerase Chain Reaction [J].
Ciasca, Maria ;
Aminoshariae, Anita ;
Jin, Ge ;
Montagnese, Thomas ;
Mickel, Andre .
JOURNAL OF ENDODONTICS, 2012, 38 (04) :486-489
[7]   Comprehensive human genome amplification using multiple displacement amplification [J].
Dean, FB ;
Hosono, S ;
Fang, LH ;
Wu, XH ;
Faruqi, AF ;
Bray-Ward, P ;
Sun, ZY ;
Zong, QL ;
Du, YF ;
Du, J ;
Driscoll, M ;
Song, WM ;
Kingsmore, SF ;
Egholm, M ;
Lasken, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (08) :5261-5266
[8]   Powering the programmed nanostructure and function of gold nanoparticles with catenated DNA machines [J].
Elbaz, Johann ;
Cecconello, Alessandro ;
Fan, Zhiyuan ;
Govorov, Alexander O. ;
Willner, Itamar .
NATURE COMMUNICATIONS, 2013, 4
[9]   Label-free optical bifunctional oligonucleotide probe for homogeneous amplification detection of disease markers [J].
Feng, Kejun ;
Qiu, Li-Ping ;
Yang, Yifeng ;
Wu, Zai-Sheng ;
Shen, Guo-Li ;
Yu, Ru-Qin .
BIOSENSORS & BIOELECTRONICS, 2011, 29 (01) :66-75
[10]   A Highly Sensitive Target-Primed Rolling Circle Amplification (TPRCA) Method for Fluorescent in Situ Hybridization Detection of MicroRNA in Tumor Cells [J].
Ge, Jia ;
Zhang, Liang-Liang ;
Liu, Si-Jia ;
Yu, Ru-Qin ;
Chu, Xia .
ANALYTICAL CHEMISTRY, 2014, 86 (03) :1808-1815