Amplified detection of nucleic acid by G-quadruplex based hybridization chain reaction

被引:97
|
作者
Dong, Juan [2 ]
Cui, Xin [2 ]
Deng, Yun [1 ]
Tang, Zhuo [2 ]
机构
[1] Chengdu Univ TCM, State Key Lab Breeding Base Systemat Reseach Dev, Chengdu 611137, Peoples R China
[2] Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2012年 / 38卷 / 01期
关键词
Hybridization chain reaction; G-quadruplex; GQ-HCR; Visual chip; PCR plus GQ-HCR; PEROXIDASE-ACTIVITY; CATALYTIC DNA; AMPLIFICATION; ENZYME; COMPLEX;
D O I
10.1016/j.bios.2012.05.042
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A protein-free, isothermal, self-amplified nucleic acid sensing system which was a G-quadruplex integrated hybridization chain reaction (GQ-HCR) system was developed. The G-quadruplex was closed two-thirds in the loop and one-third in the stem of one of the GQ-HCR hairpin probes. In the absence of the target molecule, the GQ-HCR probes stayed as inactive meta-stable hairpin structures and the G-quadruplex was inert. Reversely, the GQ-HCR probes could be cross-opened to start a hybridization chain reaction and the closed G-quadruplex could be released to be free when the GQ-HCR probes came across the target molecule. The GQ-HCR nucleic acid sensing system could detect as low as 7.5 nM ssDNA or RNA by the colorimetric method and 4 nM ssDNA by the fluorometric method. Less than 10 copies of dsDNA template could also be detected when PCR was combined with the GQ-HCR system (PCR+GQ-HCR). Because of these advantages, the GQ-HCR system was also studied for application in visual chip detection to obtain a satisfactory repeatable and specific result. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:258 / 263
页数:6
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