在 miRNA 信号转导过程中,交叉修饰-关联分层等温扩增编程逐步激活成簇的正则间隔短回文重复序列/Cas12a。

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Analytical Chemistry Pub Date : 2024-09-03 Epub Date: 2024-08-22 DOI:10.1021/acs.analchem.4c02795
Qi Wang, Juan Xia, Chengying Yang, Xiumei Chen, Baoqiang Chen, Yang Li, Hong Huang, Bingyong Lin, Longhua Guo, Jianguo Xu
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引用次数: 0

摘要

级联等温核酸扩增法整合了几种不同的扩增方案以提高检测性能,被广泛应用于生物传感领域,尤其是用于检测与肿瘤发生和发展相关的重要生物标志物--微RNA(miRNA)。然而,如何在高扩增效率和简便设计之间取得平衡仍然是一个挑战。因此,既能实现高扩增效率,又不显著增加复杂性的方法备受青睐。在这项研究中,我们提出了一种新型的 miRNA 检测方法,采用交叉引物连接分层等温扩增法(CP-HIA)逐步激活簇状规则间隔短回文重复序列(CRISPR)/Cas12a 系统。CP-HIA方法战略性地结合了n-RCA(nicking-rolling circle amplification)和p-CSDA(palindrome-aided circular strand displacement amplification),用于检测miRNA。值得注意的是,这种方法只使用了两个主要探针。它的关键创新在于交互式交叉引物策略,即 n-RCA 的扩增产物被循环利用,进一步驱动 p-CSDA,反之亦然。这种互动过程建立了分层扩增,极大地丰富了活化探针,促进了 CRISPR/Cas12a 的逐步活化和随后的目标信号扩增。因此,该方法大大提高了分析性能,包括检测低浓度 miRNA 的高灵敏度和特异性。因此,可以定量检测低至 1.06 fM 的 miRNA,miRNA 的线性响应为 10 fM 至 10 nM。这些特点证明了它在早期疾病诊断和监测方面的潜力。我们预计 CP-HIA 方法将成为开发生物医学研究先进分子诊断工具的一个前景广阔的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cross-Priming-Linked Hierarchical Isothermal Amplification Programming Progressive Activating Clustered Regularly Interspaced Short Palindromic Repeats/Cas12a in miRNA Signaling.

Cross-Priming-Linked Hierarchical Isothermal Amplification Programming Progressive Activating Clustered Regularly Interspaced Short Palindromic Repeats/Cas12a in miRNA Signaling.

Cascade isothermal nucleic acid amplification, which integrates several different amplification protocols to enhance the assay performance, is widely utilized in biosensing, particularly for detecting microRNAs (miRNAs), crucial biomarkers associated with tumor initiation and progression. However, striking a balance between a high amplification efficiency and simplicity in design remains a challenge. Therefore, methods achieving high amplification efficiency without significantly increasing complexity are highly favored. In this study, we propose a novel approach for miRNA detection, employing cross-priming-linked hierarchical isothermal amplification (CP-HIA) to progressively activate the clustered regularly interspaced short palindromic repeats (CRISPR)/Cas12a system. The CP-HIA method strategically combines nicking-rolling circle amplification (n-RCA) and palindrome-aided circular strand displacement amplification (p-CSDA) for miRNA detection. Remarkably, this method utilizes only two main probes. Its key innovation lies in the interactive cross-priming strategy, wherein the amplification product from n-RCA is recycled to further drive p-CSDA, and vice versa. This interactive process establishes a hierarchical amplification, significantly enriching the activation probes for progressive CRISPR/Cas12a activation and subsequent target signal amplification. Consequently, the method exhibits greatly enhanced analytical performance, including high sensitivity and specificity in detecting low concentrations of miRNA. As low as 1.06 fM miRNA can thus be quantitatively detected, and the linear response of the miRNA is from 10 fM to 10 nM. These features demonstrate its potential for early disease diagnosis and monitoring. We anticipate that the CP-HIA method will serve as a promising platform for developing advanced molecular diagnostic tools for biomedical research.

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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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