Suppr超能文献

仿生芯片增强的基于功能 DNA 调控的时 gated 发光 CRISPR-Cas12a 生物传感器。

Biomimetic Chip Enhanced Time-Gated Luminescent CRISPR-Cas12a Biosensors under Functional DNA Regulation.

机构信息

Hubei Province Key Laboratory of Occupational Hazard Identification and Control, School of Public Health, Medical College, Wuhan University of Science and Technology, Wuhan, 430065, People's Republic of China.

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, 430072, People's Republic of China.

出版信息

Anal Chem. 2021 Sep 21;93(37):12514-12523. doi: 10.1021/acs.analchem.1c01403. Epub 2021 Sep 7.

Abstract

Despite that the currently discovered CRISPR-Cas12a system is beneficial for improving the detection accuracy and design flexibility of luminescent biosensors, there are still challenges to extend target species and strengthen adaptability in complicated biological media. To conquer these obstacles, we present here some useful strategies. For the former, the limitation to nucleic acids assay is broken through by introducing a simple functional DNA regulation pathway to activate the unique trans-cleavage effect of this CRISPR system, under which the expected biosensors are capable of effectively transducing a protein (employing dual aptamers) and a metal ion (employing DNAzyme). For the latter, a time-gated luminescence resonance energy transfer imaging manner using a long-persistent nanophosphor as the energy donor is performed to completely eliminate the background interference and a nature-inspired biomimetic periodic chip constructed by photonic crystals is further combined to enhance the persistent luminescence. In line with the above efforts, the improved CRISPR-Cas12a luminescent biosensor not only exhibits a sound analysis performance toward the model targets (carcinoembryonic antigen and Na) but also owns a strong anti-interference feature to actualize accurate sensing in human plasma samples, offering a new and applicative analytical tool for laboratory medicine.

摘要

尽管目前发现的 CRISPR-Cas12a 系统有利于提高发光生物传感器的检测精度和设计灵活性,但在复杂的生物介质中扩展目标物种和增强适应性仍然存在挑战。为了克服这些障碍,我们在这里提出了一些有用的策略。对于前者,通过引入一种简单的功能性 DNA 调控途径来打破核酸检测的局限性,激活该 CRISPR 系统的独特的转切割效应,在此基础上,预期的生物传感器能够有效地转导一种蛋白质(采用双适体)和一种金属离子(采用 DNA 酶)。对于后者,采用长余辉纳米磷光体作为能量供体的时间门控发光共振能量转移成像方式来完全消除背景干扰,并进一步结合基于光子晶体的仿生周期性芯片来增强持久发光。通过上述努力,改进的 CRISPR-Cas12a 发光生物传感器不仅对模型靶标(癌胚抗原和 Na)表现出良好的分析性能,而且具有很强的抗干扰特性,能够在人血浆样本中实现准确检测,为临床检验医学提供了一种新的实用分析工具。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验