Amplification-free CRISPR/Cas based dual-enzymatic colorimetric nucleic acid biosensing device.

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS
Lab on a Chip Pub Date : 2025-01-08 DOI:10.1039/d4lc01039f
Guodong Tong, Pabitra Nath, Yuki Hiruta, Daniel Citterio
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引用次数: 0

Abstract

Nucleic acid testing (NAT) is widely considered the gold standard in analytical fields, with applications spanning environmental monitoring, forensic science and clinical diagnostics, among others. However, its widespread use is often constrained by complicated assay procedures, the need for specialized equipment, and the complexity of reagent handling. In this study, we demonstrate a fully integrated 3D-printed biosensensing device employing a CRISPR/Cas12a-based dual-enzymatic mechanism for highly sensitive and user-friendly nucleic acid detection. A plastic probe stick was designed to host small-sized gold nanoparticles, enhancing enzyme labeling density. Alkaline phosphatase (ALP) was then conjugated via single-stranded DNA, requiring only a single enzyme substrate addition to generate a simple visual signal change. This approach eliminates the need for amplification or centrifugation steps, achieving a limit of detection (LOD) as low as 10 pM - among the highest sensitivities reported for amplification-free colorimetric nucleic acid detection. Furthermore, we developed a device that incorporates this probe stick, integrates all necessary reagents, and features a smartphone-compatible accessory for quantitative analysis. This allows end-users to perform visual or quantitative DNA analysis with simple operations, achieving a visual detection limit of approximately 100 pM, comparable to other CRISPR-based non-amplified nucleic acid detection methods. Additionally, the system successfully distinguished perfectly matched from mismatched nucleic acid sequences, demonstrating its specificity and versatility. Although certain design limitations affected the sensitivity of the integrated device compared to the probe stick alone, the simplicity and portability of this device make it a promising tool for rapid nucleic acid screening in clinical diagnostics, environmental monitoring, and food safety control. This study paves the way for the development of practical biosensors for point-of-care testing (POCT) applications.

无扩增CRISPR/Cas双酶比色核酸生物传感装置。
核酸检测(NAT)被广泛认为是分析领域的金标准,其应用范围涵盖环境监测、法医学和临床诊断等领域。然而,它的广泛使用往往受到复杂的分析程序,需要专门的设备和试剂处理的复杂性的限制。在这项研究中,我们展示了一个完全集成的3d打印生物传感装置,采用基于CRISPR/ cas12的双酶机制进行高灵敏度和用户友好的核酸检测。设计了一种塑料探针棒来承载小尺寸的金纳米颗粒,提高酶标记密度。然后通过单链DNA偶联碱性磷酸酶(ALP),只需添加单一酶底物即可产生简单的视觉信号变化。该方法消除了扩增或离心步骤的需要,实现了低至10 pM的检测限(LOD),是无扩增比色核酸检测报告的最高灵敏度之一。此外,我们开发了一种设备,该设备集成了该探针棒,集成了所有必要的试剂,并具有智能手机兼容的定量分析配件。这使得最终用户可以通过简单的操作进行视觉或定量DNA分析,达到约100 pM的视觉检测限,与其他基于crispr的非扩增核酸检测方法相当。此外,该系统成功地区分了完全匹配和不匹配的核酸序列,证明了其特异性和通用性。虽然与单独的探针棒相比,某些设计限制影响了集成设备的灵敏度,但该设备的简单性和便携性使其成为临床诊断,环境监测和食品安全控制中快速核酸筛查的有希望的工具。这项研究为开发用于即时检测(POCT)应用的实用生物传感器铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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