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基于 DNA 结构和 CRISPR-Cas12a 的整合,用于检测前列腺特异性抗原的高灵敏荧光适体传感器。

A highly sensitive fluorescent aptasensor for detection of prostate specific antigen based on the integration of a DNA structure and CRISPR-Cas12a.

机构信息

Targeted Drug Delivery Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran; Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.

Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Anal Chim Acta. 2022 Aug 1;1219:340031. doi: 10.1016/j.aca.2022.340031. Epub 2022 Jun 3.

Abstract

Herein, a facile fluorescent CRISPR-Cas12a-based sensing strategy is presented for prostate specific antigen (PSA), as a prostate cancer biomarker, with the assistance of a cruciform DNA nanostructure and PicoGreen (PG) as a fluorochrome. Highly sensitive recognition of PSA is one of the virtues of the proposed method which comes from the use of unique features of both CRISPR-Cas12a and DNA structure in the design of the aptasensor. The presence of PSA creates a cruciform DNA nanostructure in the sample which can be loaded by PG and make sharp fluorescence emission. While, when there is no PSA, the CRISPR-Cas12a digests sequences 1 and 3 as single-stranded DNAs, causing no DNA structure and a negligible fluorescence is detected after addition of PG. This aptasensor presents a sensitive recognition performance with detection limit of 4 pg/mL and a practical use for determination of PSA in serum samples. So, this analytical strategy introduces a convenient and highly sensitive approach for detection of disease biomarkers.

摘要

本文提出了一种基于 CRISPR-Cas12a 的简便荧光传感策略,用于检测前列腺特异性抗原 (PSA),作为前列腺癌的生物标志物,该策略借助于十字形 DNA 纳米结构和 PicoGreen (PG) 作为荧光染料。该方法具有高度灵敏的 PSA 识别能力,这是因为在设计适体传感器时利用了 CRISPR-Cas12a 和 DNA 结构的独特特性。当存在 PSA 时,样品中会形成十字形 DNA 纳米结构,PG 可以负载该结构并产生尖锐的荧光发射。而当没有 PSA 时,CRISPR-Cas12a 将序列 1 和 3 消化成单链 DNA,导致没有 DNA 结构,加入 PG 后几乎检测不到荧光。该适体传感器具有灵敏的识别性能,检测限为 4 pg/mL,可用于血清样品中 PSA 的实际测定。因此,该分析策略为疾病生物标志物的检测提供了一种简便、灵敏的方法。

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