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通过 DNA 酶级联触发的 DNA 夹实现灵敏且无需酶的检测和分离。

Sensitive and Enzyme-Free Detection and Isolation via DNAzyme Cascade Triggered DNA Tweezer.

机构信息

Department of Urology, People's Hospital of Chongqing Liang Jiang New Area, Chongqing, 401147, P.R. China.

Medical insurance pricing department, People's Hospital Of Chongqing Liang Jiang New Area, Chongqing, 401147, P.R. China.

出版信息

J Microbiol Biotechnol. 2024 Sep 28;34(9):1919-1925. doi: 10.4014/jmb.2407.07006. Epub 2024 Aug 9.

DOI:10.4014/jmb.2407.07006
PMID:39187451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11473567/
Abstract

Effective isolation and sensitive detection of () is crucial for the early diagnosis and prognosis of various diseases, such as urinary tract infections. However, efficient isolation and simultaneous detection of remains a huge challenge. Herein, we depict a novel fluorescence assay for sensitive, enzyme-free detection of by integrating DNAzyme cascade-induced DNA tweezers and magnetic nanoparticles (MNPs)-based separation. The capture probe@MNPs is capable of accurately identifying target bacteria and transporting the bacteria signal to nucleic acid signals. Based on the DNAzyme cascade-induced DNA tweezers, the nucleic acid signals are extensively amplified, endowing the method with a high sensitivity and a low detection limit of 1 cfu/mL. In addition, the method also exhibits a wide detection of six orders of magnitudes. The proposed method could be extended to other bacteria detection by simply changing the aptamer sequence. Taking the merit of the high sensitivity, greatly minimized detection time (less than 1.5 h), enzyme-free characteristics, and stability, the proposed method could be potentially applied to diagnosing and preventing diseases caused by pathogenic bacteria.

摘要

有效隔离和敏感检测 () 对于各种疾病的早期诊断和预后至关重要,例如尿路感染。然而,有效地分离和同时检测 仍然是一个巨大的挑战。在此,我们描述了一种新颖的荧光分析方法,通过整合 DNA 酶级联诱导的 DNA 夹和基于磁性纳米粒子 (MNP) 的分离,用于灵敏、无酶检测 。带有 MNPs 的捕获探针@能够准确识别靶细菌,并将细菌信号传输到核酸信号。基于 DNA 酶级联诱导的 DNA 夹,核酸信号被广泛放大,赋予该方法高灵敏度和低检测限为 1 cfu/mL。此外,该方法还表现出六个数量级的宽检测范围。通过简单改变适体序列,该方法可以扩展到其他细菌的检测。鉴于高灵敏度、大大缩短的检测时间(少于 1.5 小时)、无酶特性和稳定性的优点,该方法可潜在应用于诊断和预防由病原菌引起的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/09e5f3ee68a7/jmb-34-9-1919-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/1f1d1bd18a84/jmb-34-9-1919-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/9790fd1c063c/jmb-34-9-1919-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/24c27ffc60d2/jmb-34-9-1919-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/c6fe62138530/jmb-34-9-1919-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/09e5f3ee68a7/jmb-34-9-1919-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/1f1d1bd18a84/jmb-34-9-1919-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/9790fd1c063c/jmb-34-9-1919-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/24c27ffc60d2/jmb-34-9-1919-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/c6fe62138530/jmb-34-9-1919-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1cd/11473567/09e5f3ee68a7/jmb-34-9-1919-f5.jpg

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本文引用的文献

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