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级联信号放大通过目标触发适体酶的形成用于 ATP 的灵敏电化学检测。

Cascaded signal amplification via target-triggered formation of aptazyme for sensitive electrochemical detection of ATP.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

School of Chemistry and Chemical Engineering, Chongqing University of Technology, Chongqing 400054, PR China.

出版信息

Biosens Bioelectron. 2018 Apr 15;102:296-300. doi: 10.1016/j.bios.2017.11.005. Epub 2017 Nov 20.

DOI:10.1016/j.bios.2017.11.005
PMID:29156404
Abstract

The construction of reliable sensors for adenosine triphosphate (ATP) detection gains increasing interest because of its important roles in various enzymatic activities and biological processes. Based on a cascaded, significant signal amplification approach by the integration of the aptazymes and catalytic hairpin assembly (CHA), we have developed a sensitive electrochemical sensor for the detection of ATP. The target ATP leads to the conformational change of the aptazyme sequences and their association with the hairpin substrates to form active aptazymes, in which the hairpin substrates are cyclically cleaved by the metal ion cofactors in buffer to release the enzymatic sequences that can also bind the hairpin substrates to generate active DNAzymes. The catalytic cleavage of the hairpin substrates in the aptazymes/DNAzymes thus results in the generation of a large number of intermediate sequences. Subsequently, these intermediate sequences trigger catalytic capture of many methylene blue-tagged signal sequences on the electrode surface through CHA, producing significantly amplified current response for sensitive detection of ATP at 0.6nM. Besides, the developed sensor can discriminate ATP from analogous interference molecules and be applied to human serum samples, making the sensor a useful addition to the arena for sensitive detection of small molecules.

摘要

由于三磷酸腺苷 (ATP) 在各种酶活性和生物过程中的重要作用,构建可靠的 ATP 检测传感器引起了越来越多的关注。基于级联的、显著信号放大方法,通过将适体酶和催化发夹组装 (CHA) 集成,我们开发了一种用于检测 ATP 的灵敏电化学传感器。目标 ATP 导致适体酶序列的构象变化,并与发夹底物结合形成活性适体酶,其中发夹底物在缓冲液中被金属离子辅因子周期性切割,释放出也能与发夹底物结合生成活性 DNA 酶的酶序列。适体酶/DNA 酶中发夹底物的催化切割导致大量中间序列的产生。随后,这些中间序列通过 CHA 触发电极表面上许多亚甲基蓝标记的信号序列的催化捕获,产生显著放大的电流响应,从而实现对 0.6nM 低浓度 ATP 的灵敏检测。此外,所开发的传感器可以区分 ATP 与类似的干扰分子,并应用于人血清样本,使传感器成为小分子灵敏检测领域的有用补充。

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