基于金纳米颗粒形成的y形结构和催化发夹自组装的microRNA-378比色检测。

IF 4.9 3区 工程技术 Q1 CHEMISTRY, ANALYTICAL
Yahui Gao, Jinru Pan, Bingyuan Fan, Shan Wang, Qian Wang, Wanru Liu, Fang Hu, Wei Meng
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引用次数: 0

摘要

及时和准确地发现癌症对于预防疾病进展和早期治疗确诊病例至关重要。mirna是癌症标志物。本研究提出了一种简单的miRNA检测方法。结合催化发夹组装核酸扩增技术,设计了三种纳米金发夹。采用低ph法进行快速耦合,并用miR-378打开发夹H1,触发循环反应和信号放大,最终形成y形结构,从而缩小金纳米颗粒之间的距离,实现比色检测。吸光度变化(A620/A520)与miR-378浓度成正比(0.05-5 nM),检出限为0.05 nM。该方法对实际样品也有明显的检测效果。用该方法对HeLa和L-02细胞提取物进行分析。前者没有明显的颜色变化,而后者的最大吸收峰出现了红移,颜色由红色变为紫色。HeLa细胞能检测到的最小细胞数为500个细胞/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Colorimetric Detection of microRNA-378 Based on Y-Shaped Structure Formed by Gold Nanoparticles and Catalytic Hairpin Self-Assembly.

The timely and accurate detection of cancer is crucial for preventing disease progression and for the early treatment of confirmed cases. MiRNAs are cancer markers. In this study, a simple miRNA detection method is proposed. Three hairpins were designed based on gold nanoparticles combined with catalytic hairpin assembly nucleic acid amplification technology. The low-pH method was used for rapid coupling, and hairpin H1 was opened by miR-378, triggering the cycle reaction and signal amplification and finally forming a Y-shaped structure, thereby narrowing the distance between gold nanoparticles and achieving colorimetric detection. The absorbance change (A620/A520) was proportional to the concentration of miR-378 (0.05-5 nM), with a detection limit of 0.05 nM. This method also has an evident detection effect on real samples. HeLa and L-02 cell extracts were analyzed using this method. The former showed no obvious color change, whereas the maximum absorption peak of the latter showed a red shift, and the color changed from red to purple. The minimum number of cells that could be detected using HeLa cells was 500 cells/mL.

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来源期刊
Biosensors-Basel
Biosensors-Basel Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
6.60
自引率
14.80%
发文量
983
审稿时长
11 weeks
期刊介绍: Biosensors (ISSN 2079-6374) provides an advanced forum for studies related to the science and technology of biosensors and biosensing. It publishes original research papers, comprehensive reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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