Direct fluorescence detection of microRNA based on enzymatically engineered primer extension poly-thymine (EPEPT) reaction using copper nanoparticles as nano-dye

被引:48
作者
Chi, Bao-Zhu
Liang, Ru-Ping [1 ]
Qiu, Wei-Bin
Yuan, Yan-Hong
Qiu, Jian-Ding [1 ]
机构
[1] Nanchang Univ, Coll Chem, Nanchang 330031, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA; PolyT-CuNPs; KFexo(-); TdTase; Fluorescence detection; DSDNA-TEMPLATED FORMATION; ROLLING CIRCLE AMPLIFICATION; CELL LUNG-CANCER; STRATEGY; NANOCLUSTERS; GENE; QUANTIFICATION; POLYMERIZATION; EXPRESSION; MIR-21;
D O I
10.1016/j.bios.2016.08.042
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new strategy based on enzymatically engineered primer extension poly-thymine (EPEPT) and nano materials in situ generation technology is reported for direct detection of microRNA (miRNA) in a fluorescence turn-on format using the sequential and complementary reactions catalyzed by Klenow Fragment exo(-) (KFexo(-)) and terminal deoxynucleotidyl transferase (TdTase). The short miRNA can be efficiently converted into long poly-thymine (polyT) sequences, which function as template for in situ formation of fluorescence copper nanoparticles (CuNPs) as nano-dye for detecting miRNA. The polyT-CuNPs can effectively form and emit intense red fluorescence under the 340 nm excitation. For the proof of concept, microRNA-21 (miR-21) was selected as the model target to testify this strategy as a versatile assay platform. By directly using miR-21 as the primer, the simple, rapid and sensitive miRNA detection was successfully achieved with a good linearity between 1 pM and 1 nM and a detection limit of 100 fM. Thus, the EPEPT strategy holds great potential in biochemical sensing research as an efficient and universal platform. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 221
页数:6
相关论文
共 41 条
[1]  
Bollum F.J., 1974, The Enzymes, V10, P145
[2]   Ultrasmall Copper Nanoparticles Synthesized with a Plant Tea Reducing Agent [J].
Brumbaugh, Aaron D. ;
Cohen, Katelyn A. ;
St Angelo, Sarah K. .
ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2014, 2 (08) :1933-1939
[3]   Real-time quantification of microRNAs by stem-loop RT-PCR [J].
Chen, CF ;
Ridzon, DA ;
Broomer, AJ ;
Zhou, ZH ;
Lee, DH ;
Nguyen, JT ;
Barbisin, M ;
Xu, NL ;
Mahuvakar, VR ;
Andersen, MR ;
Lao, KQ ;
Livak, KJ ;
Guegler, KJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e179.1-e179.9
[4]   Random dsDNA-templated formation of copper nanoparticles as novel fluorescence probes for label-free lead ions detection [J].
Chen, Junhua ;
Liu, Jie ;
Fang, Zhiyuan ;
Zeng, Lingwen .
CHEMICAL COMMUNICATIONS, 2012, 48 (07) :1057-1059
[5]   Highly Sensitive Determination of microRNA Using Target-Primed and Branched Rolling-Circle Amplification [J].
Cheng, Yongqiang ;
Zhang, Xian ;
Li, Zhengping ;
Jiao, Xiaoxia ;
Wang, Yucong ;
Zhang, Yali .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (18) :3268-3272
[6]   Sensitive and homogeneous microRNA detection using branched cascade enzymatic amplification [J].
Chi, Bao-Zhu ;
Liang, Ru-Ping ;
Zhang, Li ;
Qiu, Jian-Ding .
CHEMICAL COMMUNICATIONS, 2015, 51 (52) :10543-10546
[7]   Toehold-initiated Rolling Circle Amplification for Visualizing Individual MicroRNAs In Situ in Single Cells [J].
Deng, Ruijie ;
Tang, Longhua ;
Tian, Qianqian ;
Wang, Ying ;
Lin, Lei ;
Li, Jinghong .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2014, 53 (09) :2389-2393
[8]   Biochemical, structural, and physiological characterization of terminal deoxynucleotidyl transferase [J].
Fowler, Jason D. ;
Suo, Zucai .
CHEMICAL REVIEWS, 2006, 106 (06) :2092-2110
[9]   Gene regulation by transcription factors and microRNAs [J].
Hobert, Oliver .
SCIENCE, 2008, 319 (5871) :1785-1786
[10]   MicroRNA gene expression deregulation in human breast cancer [J].
Iorio, MV ;
Ferracin, M ;
Liu, CG ;
Veronese, A ;
Spizzo, R ;
Sabbioni, S ;
Magri, E ;
Pedriali, M ;
Fabbri, M ;
Campiglio, M ;
Ménard, S ;
Palazzo, JP ;
Rosenberg, A ;
Musiani, P ;
Volinia, S ;
Nenci, I ;
Calin, GA ;
Querzoli, P ;
Negrini, M ;
Croce, CM .
CANCER RESEARCH, 2005, 65 (16) :7065-7070