放大器
滚动圆复制
DNA
聚合酶链反应
核酸
计算生物学
信号(编程语言)
序列(生物学)
基序列
模板
杂交探针
复式(建筑)
碱基对
生物
生物系统
计算机科学
遗传学
纳米技术
材料科学
基因
聚合酶
程序设计语言
作者
Bingjie Zou,Yinjiao Ma,Haiping Wu,Guohua Zhou
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2011-12-08
卷期号:137 (3): 729-734
被引量:17
摘要
Detection of nucleic acids with signal amplification is preferable in clinical diagnosis. A novel approach was developed for signal amplification by coupling invasive reaction with hyperbranched rolling circle amplification (HRCA). Invasive reaction, which does not rely on specific recognition sequences in a target but a specific structure formed by the specific binding of an upstream probe and a downstream probe to a target DNA, can generate thousands of flaps from one target DNA; then the flaps are ligated with padlock probes to form circles, which are the templates of HRCA. As HRCA amplicon sequence is free of target DNA sequence, signal amplification is achieved. Because flap sequence is the same to any target of interest, HRCA is universal; the detection cost is hence greatly reduced. The sensitivity of the proposed method is less than 1 fM artificial DNA targets; and the specificity of the method is high enough to discriminate one base difference in the target sequence. The feasibility was verified by detecting real biological samples from HBV carriers, indicating that the method is highly sensitive, cost-effective, and has a low risk of cross-contamination from amplicons. These properties should give great potential in clinical diagnosis.
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