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增强型 3D DNA walker 诱导的 CRISPR/Cas12a 技术用于高灵敏度检测与骨质疏松症相关的外泌体 miRNA。

Enhancing 3D DNA Walker-Induced CRISPR/Cas12a Technology for Highly Sensitive Detection of ExomicroRNA Associated with Osteoporosis.

机构信息

Department of Laboratory Medicine, The Third Affiliated Hospital of Chongqing Medical University, Chongqing 401120, PR China.

Department of Gerontology, The First Branch of The First Affiliated Hospital of Chongqing Medical University, Chongqing 400000, PR China.

出版信息

ACS Sens. 2024 Mar 22;9(3):1438-1446. doi: 10.1021/acssensors.3c02533. Epub 2024 Mar 7.

DOI:10.1021/acssensors.3c02533
PMID:38451610
Abstract

Exosomal microRNAs (exomiRNAs) have emerged as promising biomarkers for the early clinical diagnosis of osteoporosis. However, their limited abundance and short length in peripheral blood present significant challenges for the accurate detection of exomiRNAs. Herein, we have designed and implemented an efficacious fluorescence-based biosensor for the highly sensitive detection of exomiRNA associated with osteoporosis, leveraging the enhancing 3D DNA walker-induced CRISPR/Cas12a technology. The engineered DNA walker is capable of efficiently transforming target exomiRNA into amplifying DNA strands, thereby enhancing the sensitivity of the developed biosensor. Concurrently, the liberated DNA strands serve as activators to trigger Cas12a -cleavage activity, culminating in a significantly amplified fluorescent signal for the highly sensitive detection of exomiRNA-214. Under optimal conditions, the devised technology demonstrated the capacity to detect target exomiRNA-214 at concentrations as low as 20.42 fM, encompassing a wide linear range extending from 50.0 fM to 10.0 nM. Moreover, the fluorescence-based biosensor could accurately differentiate between healthy individuals and osteoporosis patients via the detection of exomiRNA-214, which was in agreement with RT-qPCR results. As such, this biosensing technology offers promise as a valuable tool for the early diagnosis of osteoporosis.

摘要

外泌体 microRNAs(exomiRNAs)已成为骨质疏松症早期临床诊断有希望的生物标志物。然而,它们在外周血中的丰度有限且长度较短,这给 exomiRNAs 的准确检测带来了重大挑战。在此,我们设计并实施了一种有效的基于荧光的生物传感器,用于高度敏感地检测与骨质疏松症相关的 exomiRNA,利用增强的 3D DNA walker 诱导的 CRISPR/Cas12a 技术。工程化的 DNA walker 能够有效地将靶标 exomiRNA 转化为扩增 DNA 链,从而提高了开发的生物传感器的灵敏度。同时,释放的 DNA 链作为激活物触发 Cas12a 切割活性,最终产生高度灵敏检测 exomiRNA-214 的显著放大荧光信号。在最佳条件下,所设计的技术能够以低至 20.42 fM 的浓度检测靶标 exomiRNA-214,线性范围从 50.0 fM 到 10.0 nM 很宽。此外,通过检测 exomiRNA-214,荧光生物传感器可以准确地区分健康个体和骨质疏松症患者,这与 RT-qPCR 结果一致。因此,这种基于生物传感的技术有望成为骨质疏松症早期诊断的有价值工具。

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