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A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor

It has recently been discovered that, like other members of the Cas family (12a and 13a), the clustered regularly interspaced short palindrome repeat CRISPR-Cas14a system not only mediates high-sensitivity detection with exceptionally strong gene editing ability but is also generally useful for DNA...

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Autores principales: Wang, Yu, Peng, Yuan, Zhou, Huanying, Gao, Zhixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601294/
https://www.ncbi.nlm.nih.gov/pubmed/37880670
http://dx.doi.org/10.1186/s12951-023-02163-z
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author Wang, Yu
Peng, Yuan
Zhou, Huanying
Gao, Zhixian
author_facet Wang, Yu
Peng, Yuan
Zhou, Huanying
Gao, Zhixian
author_sort Wang, Yu
collection PubMed
description It has recently been discovered that, like other members of the Cas family (12a and 13a), the clustered regularly interspaced short palindrome repeat CRISPR-Cas14a system not only mediates high-sensitivity detection with exceptionally strong gene editing ability but is also generally useful for DNA detection via fluorescence. Photoelectrochemical (PEC) sensors have been widely applied as efficient analytical tools. Measuring electrical signals is more cost-effective and the necessary equipment is more easily portable than fluorescence signal detectors, but their stability still needs to be improved. The high base resolution of CRISPR-Cas14a can compensate for such shortcomings. Therefore, electrical signals and fluorescence signals were combined, and the development of a universal CRISPR-Cas14a-responsive ultrasensitive upconversion PEC sensor is described in this paper. Moreover, strand displacement amplification (SDA) and a near-infrared (NIR) light source were utilized to further improve the stability and sensitivity of the photoelectric signals. At the same time, the modified working electrode (UCNPs-ssDNA-CdS@Au/ITO) on the three-electrode disposable sensor was used as the reporter probe, which cooperates with the trans-cleavage activity of Cas14a endonuclease. To verify the universality of this sensor, the UCNPs-Cas14a-based PEC sensor was applied for the detection of the small-molecule toxin T2 and protein kinase PTK7. Here, we report that the limit of detection of this reagent was within the fg range, successfully applied to the detection of T2 in oats and PTK7 in human serum. We propose that by combining PEC and CRISPR-14a, UCNPs-Cas14a-based PEC sensors could become powerful drivers for the extensive development of ultrasensitive, accurate and cost-effective universal sensors for detection and diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-02163-z.
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spelling pubmed-106012942023-10-27 A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor Wang, Yu Peng, Yuan Zhou, Huanying Gao, Zhixian J Nanobiotechnology Research It has recently been discovered that, like other members of the Cas family (12a and 13a), the clustered regularly interspaced short palindrome repeat CRISPR-Cas14a system not only mediates high-sensitivity detection with exceptionally strong gene editing ability but is also generally useful for DNA detection via fluorescence. Photoelectrochemical (PEC) sensors have been widely applied as efficient analytical tools. Measuring electrical signals is more cost-effective and the necessary equipment is more easily portable than fluorescence signal detectors, but their stability still needs to be improved. The high base resolution of CRISPR-Cas14a can compensate for such shortcomings. Therefore, electrical signals and fluorescence signals were combined, and the development of a universal CRISPR-Cas14a-responsive ultrasensitive upconversion PEC sensor is described in this paper. Moreover, strand displacement amplification (SDA) and a near-infrared (NIR) light source were utilized to further improve the stability and sensitivity of the photoelectric signals. At the same time, the modified working electrode (UCNPs-ssDNA-CdS@Au/ITO) on the three-electrode disposable sensor was used as the reporter probe, which cooperates with the trans-cleavage activity of Cas14a endonuclease. To verify the universality of this sensor, the UCNPs-Cas14a-based PEC sensor was applied for the detection of the small-molecule toxin T2 and protein kinase PTK7. Here, we report that the limit of detection of this reagent was within the fg range, successfully applied to the detection of T2 in oats and PTK7 in human serum. We propose that by combining PEC and CRISPR-14a, UCNPs-Cas14a-based PEC sensors could become powerful drivers for the extensive development of ultrasensitive, accurate and cost-effective universal sensors for detection and diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-02163-z. BioMed Central 2023-10-26 /pmc/articles/PMC10601294/ /pubmed/37880670 http://dx.doi.org/10.1186/s12951-023-02163-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wang, Yu
Peng, Yuan
Zhou, Huanying
Gao, Zhixian
A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
title A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
title_full A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
title_fullStr A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
title_full_unstemmed A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
title_short A universal CRISPR-Cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
title_sort universal crispr-cas14a responsive triple-sensitized upconversion photoelectrochemical sensor
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10601294/
https://www.ncbi.nlm.nih.gov/pubmed/37880670
http://dx.doi.org/10.1186/s12951-023-02163-z
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