一种新颖的多合一目标驱动熵驱动动态 DNA 网络,用于调节 CRISPR/AsCas12a 的活性以增强 DNA 检测能力

IF 5.7 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Xingrong Li, Cuixiang Wang, Jiatong Chai, Hongmao Liu, Xinli Jiang, Yumei Li, Zhiqiang Li, Yirong Li
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引用次数: 0

摘要

背景通过沃森-克里克(Watson-Crick)碱基配对的可编程性,无酶自主 DNA 纳米器件已被开发出来用于检测各种分析物。然而,与酶生物传感器相比,使用无酶 DNA 网络来创建用于检测低量目标物的生物传感器仍然受到循环次数的限制。此外,这些生物传感器仍然需要结合其他扩增策略来提高灵敏度,这就使得检测工作流程复杂化,并且缺乏一个统一兼容的系统来一锅端目标。在没有目标物的情况下,底物和crRNA之间的自主杂交因互补区的包围而受到动力学阻碍,从而导致Cas12a失去激活功能。相反,目标启动 EDN,将激活子链从双链重新配置为分支结构,这为调整与 crRNA 的杂交提供了有效手段,从而控制了 CRISPR/AsCas12a 的无差别附带切割活动。与传统的 EDN 相比,EDN 与 CRISPR 催化剂之间的协同激活可以显著提高一锅中目标的检测信号。意义和新颖性总之,这种靶标触发的 EDN 通过切换激活剂链来调节 AsCas12a(称为 TERA)的活性,其灵敏度比传统的 Cas12a 单独检测高出两个数量级以上,从而形成了一种可设计的通用 CRISPR 传感平台,有利于快速、稳健和一次过检测核分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Novel All-in-one Target-Powered Entropy-Driven Dynamic DNA Networks to Regulate the Activity of CRISPR/AsCas12a for Enhanced DNA Detection

A Novel All-in-one Target-Powered Entropy-Driven Dynamic DNA Networks to Regulate the Activity of CRISPR/AsCas12a for Enhanced DNA Detection

Background

The non-enzyme autonomous DNA nanodevices have been developed to detect various analytes through the programmability of Watson-Crick base pairing. Nevertheless, by comparison with enzymatic biosensors, the usage of enzyme-free DNA networks to create biosensors for testing low amounts of targets is still subject to the finite number of cycles. Besides, these biosensors still require the incorporation of other amplification strategies to improve the sensitivity, which complicates the detection workflow and lacks of a uniform compatible system to respond to the target in one pot.

Results

Here, we put forward a novel way for rapid and sensitive DNA diagnostic via EDN (entropy-driven dynamic network) coupling with CRISPR/AsCas12a-powered amplification. In the absence of the target, the autonomous hybridization among the substrate and crRNA is kinetically hindered by enclosing complementary regions, which leads to the loss of the activation function of Cas12a. On the contrary, the target initiates the EDN, reconfiguring the activator strand from a duplex to branch construction, which provides a valid means to adjust the hybridization with crRNA, thereby controlling the indiscriminate collateral cleavage activities of the CRISPR/AsCas12a. Compared with the traditional EDN, synergistic activation between the EDN and the CRISPR catalyst could dramatically enhance the detection signal of the target in one pot. Furthermore, the proposed approach provides universal platforms through the rational functional and structural design of DNA assembly modules.

Significance and Novelty

Overall, this target-triggered EDN switches the activator strand to regulate the activity of AsCas12a (called TERA), which showed more than two orders of magnitude sensitivity than the conventional Cas12a alone assay, resulting in a devisable universal CRISPR sensing platform that favours the fast, robust and one-pot detection of nucleic molecules.
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来源期刊
Analytica Chimica Acta
Analytica Chimica Acta 化学-分析化学
CiteScore
10.40
自引率
6.50%
发文量
1081
审稿时长
38 days
期刊介绍: Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.
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