首页 | 本学科首页   官方微博 | 高级检索  
     检索      

基于脱氧核酶-等温级联放大耦合的传感体系高灵敏检测水样中铅离子
引用本文:陆云飞,贾敏,吴继魁.基于脱氧核酶-等温级联放大耦合的传感体系高灵敏检测水样中铅离子[J].上海海洋大学学报,2020,29(6):840-846.
作者姓名:陆云飞  贾敏  吴继魁
作者单位:上海海洋大学食品学院,上海201306;上海海洋大学食品学院,上海201306;上海水产品加工及贮藏工程技术中心,上海201306;农业农村部水产品贮藏保鲜质量安全风险评估实验室,上海201306
基金项目:国家自然科学基金;上海市自然科学基金
摘    要:我们结合等温直链替代反应(SDA)和指数扩增(EXPAR)设计了一种非标记、高灵敏的Pb2+荧光生物传感体系。在 Pb2+存在情况下,底物链被活化的GR-5 DNAzyme快速切割释放引物1。引物1与模板1杂交,并被DNA聚合酶(BSM)延伸形成带限制性内切酶(Nt.BbvCI)的识别序列的双链核苷酸。BSM从Nt.BbvCI切割产生的切口再次延伸形成双链核苷酸,并释放信号G4-DNA片段。G4-DNA片段同时又可以作为模板2的引物,启动指数放大过程,从而释放更多的信号G4-DNA片段。最后,扩增产物G4-DNA与原卟啉锌(ZnPPIX)相互结合从而产生强烈的荧光信号。我们详细优化了多种因素对检测体系的影响,在最优实验条件下,此方法对Pb2+的线性检测范围为 0.1~50 nM,检出限为0.03 nM(S/N=3),回归方程为 y=288.7x+744.7(y为荧光强度,x为Pb2+浓度)。干扰实验表明,该传感器对Pb2+具有良好的特异性和选择性。该传感体系成功应用于环境水体中 Pb2+含量检测,加标回收率为 94.0%~103.0%。本方法操作简单、选择性好、灵敏度高、有较强的抗干扰性能,可用于环境水样中Pb2+的高灵敏检测。

关 键 词:Pb2+  荧光传感器  等温信号放大  G-四联体  原卟啉锌  GR-5  DNAzyme
收稿时间:2019/5/20 0:00:00
修稿时间:2020/3/11 0:00:00

A DNAzyme-isothermal cascade amplification sensing system for ultrasensitive detection of Pb2+ in water samples
LU Yunfei,JIA Min,WU Jikui.A DNAzyme-isothermal cascade amplification sensing system for ultrasensitive detection of Pb2+ in water samples[J].Journal of Shanghai Ocean University,2020,29(6):840-846.
Authors:LU Yunfei  JIA Min  WU Jikui
Institution:Shanghai Ocean University,Shanghai Ocean University,Shanghai Ocean University
Abstract:We exploited strand displacement amplification (SDA) and exponential amplification (EXPAR) to design a label-free, ultrasensitive fluorescence sensing system for the detection of Pb2+. In the presence of Pb2+, the substrate strand is rapidly cleaved by the activated GR-5 DNAzyme to release Primer 1. Primer 1 hybridizes to template 1 and is extended by DNA polymerase (BSM) to form a double-stranded nucleotide with a recognition sequence for restriction endonuclease (Nt. BbvCI). The nicks generated by BSM cleavage from Nt. BbvCI re-extend to form double-stranded nucleotides and release the signal G4-DNA fragment. The G4-DNA fragment can also be used as a primer for template 2 to initiate a series amplification process, thereby releasing more signal G4-DNA fragments. Finally, G4-DNA binds to protoporphyrin zinc (ZnPPIX) to produce a strong fluorescent signal. The effects of various factors on the sensing system were investigated. Under the optimal experimental conditions, the linear detection range of Pb2+ was 0.1~50 nM, and the LOD was 0.03 nM (S/N=3). The regression equation is y=288.7x+744.7 (y is the fluorescence intensity and x is the Pb2+ concentration). Interference experiments show that the sensing system has good selectivity for Pb2+ against other metal ions. This method was applied to the detection of Pb2+ in environmental water, and the recoveries were obtained from 94.0% to103.0%. The proposed sensing system has the advantages of simple operation, good selectivity, high sensitivity and strong anti-interference performance, and can be used for high-sensitivity detection of Pb2+ in environmental water samples.
Keywords:Pb2+  Fluorescence sensing  Isothermal signal amplification  G-quadruplex  ZnppIX  GR-5 DNAzyme
本文献已被 万方数据 等数据库收录!
点击此处可从《上海海洋大学学报》浏览原始摘要信息
点击此处可从《上海海洋大学学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号