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基于 Cas12a 的 3D 纳米俘获物提高了反式切割效率,实现了唾液中 miRNA-31 的高灵敏和快速电化学检测。

High-sensitive and rapid electrochemical detection of miRNA-31 in saliva using Cas12a-based 3D nano-harvester with improved trans-cleavage efficiency.

机构信息

Department of Laboratory Medicine, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, 646000, China.

Department of Laboratory Medicine, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, 646000, China.

出版信息

Talanta. 2024 Jan 1;266(Pt 2):125066. doi: 10.1016/j.talanta.2023.125066. Epub 2023 Aug 10.

Abstract

Salivary miRNA-31 is a reliable diagnostic marker for early-stage oral squamous cell carcinoma (OSCC), but accurate detection of miRNA-31 in saliva samples is a challenge because of its low level and high sequence homology. The CRISPR/Cas12a system has the exceptional potential to enable simple nucleic acid analysis but suffers from low speed and sensitivity. To achieve rapid and high-sensitive detection of miRNA-31 using the CRISPR/Cas12a system, a Cas12a-based nano-harvester activated by a polymerase-driven DNA walker, named as dual 3D nanorobots, was developed. The target walked rapidly on the surface of DNA hairpin-modified magnetic nanoparticles driven by DNA polymerase, generating numerous double-strand DNA (dsDNA). Then, the Cas12a bound to the generated dsDNA for activating its trans-cleavage activity, forming 3D nano-harvester. Subsequently, the harvester cut and released methylene blue-labeled DNA hairpins immobilized on the sensing interface, leading to the change in electrochemical signal. We found that the trans-cleavage activity of the harvester was higher than the conventional CRISPR/Cas12a system. The developed dual 3D nanorobots could enable rapid (detection time within 60 min), high-sensitive (detection limit of femtomolar), and specific analysis of miRNA-31 in saliva samples. Thus, our established electrochemical biosensing strategy has great potential for early diagnosis of OSCC.

摘要

唾液中的 miRNA-31 是早期口腔鳞状细胞癌(OSCC)的可靠诊断标志物,但由于其低水平和高序列同源性,准确检测唾液中的 miRNA-31 是一个挑战。CRISPR/Cas12a 系统具有实现简单核酸分析的巨大潜力,但速度和灵敏度较低。为了使用 CRISPR/Cas12a 系统实现对 miRNA-31 的快速高灵敏检测,开发了一种基于 Cas12a 的纳米采集器,该纳米采集器由聚合酶驱动的 DNA walker 激活,称为双 3D 纳米机器人。目标物在 DNA 聚合酶驱动下在 DNA 发夹修饰的磁性纳米颗粒表面上快速移动,产生大量双链 DNA(dsDNA)。然后,Cas12a 与生成的 dsDNA 结合以激活其反式切割活性,形成 3D 纳米采集器。随后,采集器切割并释放固定在传感界面上的亚甲基蓝标记的 DNA 发夹,导致电化学信号发生变化。我们发现,采集器的反式切割活性高于传统的 CRISPR/Cas12a 系统。所开发的双 3D 纳米机器人可以实现快速(检测时间在 60 分钟内)、高灵敏(检测限为飞摩尔级)和特异性分析唾液中的 miRNA-31。因此,我们建立的电化学生物传感策略具有用于 OSCC 早期诊断的巨大潜力。

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