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CRISPR/Cas12a切割触发的纳米花用于太赫兹频率下无荧光和无靶标扩增的ctDNA生物传感

CRISPR/Cas12a cleavage triggered nanoflower for fluorescence-free and target amplification-free biosensing of ctDNA in the terahertz frequencies.

作者信息

Zhao Jingjing, Zhu Jianfang, Wang Weiqiang, Qian Zhengfang, Fan Shuting

机构信息

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University , Shenzhen 518060, China.

Institute of Health Sciences and Technology, Institutes of Material Science and Information Technology, Anhui University, Hefei 230601, China.

出版信息

Biomed Opt Express. 2024 Aug 21;15(9):5400-5410. doi: 10.1364/BOE.534511. eCollection 2024 Sep 1.

Abstract

The detection of tumor biomarkers in liquid biopsies requires high sensitivity and low-cost biosensing strategies. However, few traditional techniques can satisfy the requirements of target amplification-free and fluorescence-free at the same time. In this study, we have proposed a novel strategy for ctDNA detection with the combination of terahertz spectroscopy and the CRISPR/Cas12 system. The CRISPR/Cas12a system is activated by the target ctDNA, resulting in a series of reactions leading to the formation of an Au-Fe complex. This complex is easily extracted with magnets and when dropped onto the terahertz metamaterial sensor, it can enhance the frequency shift, providing sensitive and selective sensing of the target ctDNA. Results show that the proposed terahertz biosensor exhibits a relatively low detection limit of 0.8 fM and a good selectivity over interference species. This detection limit is improved by three orders of magnitude compared with traditional biosensing methods using terahertz waves. Furthermore, a ctDNA concentration of 100 fM has been successfully detected in bovine serum (corresponding to 50 fM in the final reaction system) without amplification.

摘要

在液体活检中检测肿瘤生物标志物需要高灵敏度和低成本的生物传感策略。然而,很少有传统技术能同时满足无需靶标扩增和无荧光的要求。在本研究中,我们提出了一种将太赫兹光谱与CRISPR/Cas12系统相结合的新型ctDNA检测策略。CRISPR/Cas12a系统被靶标ctDNA激活,引发一系列反应,导致形成金-铁复合物。这种复合物很容易用磁铁提取,当滴加到太赫兹超材料传感器上时,它可以增强频移,从而对靶标ctDNA进行灵敏且选择性的传感。结果表明,所提出的太赫兹生物传感器具有相对较低的检测限,为0.8 fM,并且对干扰物质具有良好的选择性。与使用太赫兹波的传统生物传感方法相比,该检测限提高了三个数量级。此外,在未进行扩增的情况下,已成功在牛血清中检测到浓度为100 fM的ctDNA(在最终反应体系中相当于50 fM)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9293/11407253/444926994ece/boe-15-9-5400-g001.jpg

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