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CRISPR-Cas12a-driven MXene-PEDOT:PSS piezoresistive wireless biosensor

佩多:嘘 材料科学 纳米技术 生物传感器 光电子学 图层(电子)
作者
Ruijin Zeng,Weijun Wang,Mingming Chen,Qing Wan,Caicheng Wang,Dietmar Knopp,Dianping Tang
出处
期刊:Nano Energy [Elsevier BV]
卷期号:82: 105711-105711 被引量:385
标识
DOI:10.1016/j.nanoen.2020.105711
摘要

Beyond extraordinary in vivo accurate gene editing and regulation capabilities, the CRISPR-Cas-associated biotechnology has created a new era of in vitro nucleic acid sensing due to its inherent high-efficiency enzyme cleavage activity and robustness. However, most of the existing CRISPR-Cas systems are largely involve fluorescent reporters or lateral flow strips biosensor and can't fully explore their potential applications (sensitivity and field-deployable) due to the lack of effective signal transduction and wireless data transmission with smartphone readout. Herein, a CRISPR-Cas12a-mediated instrument-free based on flexible interdigitated electrodes-modified piezoresistive block [abrasive paper-molded microstructure polydimethylsiloxane (PDMS) and MXene (Ti3C2Tx)-PEDOT:PSS film] was designed for point-of-care of human papillomavirus (HPV)-related DNA with integrated-module smartphone visual readout. Biotin/thiol-modification single-stranded DNA (ssDNA), acts as a linker between [email protected] nanoparticles ([email protected]) and streptavidin-coated magnetic bead (MB), are non-specifically cleaved by Cas12a when the guide RNA binds to the target HPV-DNA. Released and separated [email protected] efficiently catalyzes H2O2 to O2, and further compress the Ti3C2Tx-PEDOT:PSS/PDMS in a 3D-printed home-made pressure-tight vessel, thus causing the increasing current of the whole circuit thanks to contacting deformation of Ti3C2Tx-PEDOT:PSS/PDMS module and interdigital electrode. After integrating the Bluetooth device and wireless sensing technology in the circuit, the current signal of the target DNA can be wirelessly collected and recorded in real-time and further transmitted/displayed to the mobile terminal of the smartphone. This all-in-one detection mode not only bridges the technological gap between biological signal conduction, wireless transmission, and smartphone interface but also improves the portability and the sensitivity (more than one order of magnitude lower than that of traditional CRISPR-Cas12a biosensors). We expect that a powerful CRISPR-Cas12a system coupled with piezoresistive sensor with wireless transmission technology will become a great demonstration and widely used in real-time wireless biomedical analysis, portable point-of-care health monitoring, and molecular diagnostics.
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