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一种基于目标反馈滚环切割信号放大的策略,用于 miRNA 的超灵敏电化学检测,该策略使用了自组装的 CeO@Ag 杂化纳米花。

A Target-Feedback Rolling-Cleavage signal amplifier for ultrasensitive electrochemical detection of miRNA with Self-Assembled CeO@Ag hybrid nanoflowers.

机构信息

Key Laboratory of Medical Diagnostics of Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, PR China; Chongqing Medical Laboratory Microfluidics and SPRi Engineering Research Center, Chongqing Medical University, Chongqing 400016, PR China.

Key Laboratory of Medical Diagnostics of Ministry of Education, Department of Laboratory Medicine, Chongqing Medical University, Chongqing 400016, PR China.

出版信息

Bioelectrochemistry. 2022 Aug;146:108152. doi: 10.1016/j.bioelechem.2022.108152. Epub 2022 May 4.

DOI:10.1016/j.bioelechem.2022.108152
PMID:35594730
Abstract

Currently, developing an effective and easy-to-operate signal amplification assay to detect the trace-amount miRNAs in serum remains a significant challenge. Herein, an ultrasensitive CeO@Ag hybrid nanoflower (CeO@Ag HNF)-labeled electrochemical biosensor was developed for sensing miRNA, based on a target-feedback rolling-cleavage (TFRC) signal amplifier. CeO@Ag HNFs possessing a unique three-dimensional layered structure were synthesized without any complex reaction conditions, such as heating and vacuum. The bimetallic nanoflowers provided a large surface area and excellent CAT-like activity, thereby enhancing electrochemical performance. Based on the principle of branched catalytic hairpin assembly, target miRNA could continuously trigger the assembly of branched junctions with ends composed of DNAzyme. The activated DNAzyme was able to cleave the hairpin substrate efficiently and release to capture more CeO@Ag HNFs label. The process combining target-driven branched catalytic hairpin assembly and DNAzyme-assisted rolling cleavage were defined as TFRC signal amplification. This sensitive electrochemical biosensor exhibited good linear relationship of 1 fM - 1 nM with a detection limit down to 0.89 fM. The proposed method is expected to have a promising application in the miRNA-associated fundamental research and clinical diagnosis.

摘要

目前,开发一种有效且易于操作的信号放大测定法来检测血清中痕量 miRNA 仍然是一个重大挑战。在此,基于靶标反馈滚环切割(TFRC)信号放大,开发了一种超灵敏的 CeO@Ag 杂化纳米花(CeO@Ag HNF)标记电化学生物传感器来感测 miRNA。CeO@Ag HNF 具有独特的三维层状结构,无需任何复杂的反应条件(如加热和真空)即可合成。双金属纳米花提供了更大的表面积和优异的 CAT 样活性,从而增强了电化学性能。基于分支催化发夹组装的原理,靶 miRNA 可以连续触发具有由 DNA 酶组成的末端的分支接头的组装。激活的 DNA 酶可以有效地切割发夹底物并释放出更多的 CeO@Ag HNF 标签。将靶标驱动的分支催化发夹组装和 DNA 酶辅助的滚环切割过程定义为 TFRC 信号放大。这种灵敏的电化学生物传感器表现出良好的线性关系,在 1 fM - 1 nM 范围内检测限低至 0.89 fM。该方法有望在 miRNA 相关的基础研究和临床诊断中具有广阔的应用前景。

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