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用于复杂基质中蛋白质检测的DNA辅助CRISPR-Cas12a增强荧光测定法

DNA-Assisted CRISPR-Cas12a Enhanced Fluorescent Assay for Protein Detection in Complicated Matrices.

作者信息

Munusamy Sathishkumar, Zheng Haiyan, Jahani Rana, Zhou Shuo, Chen Jun, Kong Juanhua, Guan Xiyun

机构信息

Department of Chemistry, University of Missouri, Columbia, Missouri 65211, United States.

出版信息

ACS Appl Bio Mater. 2025 Jan 20;8(1):754-762. doi: 10.1021/acsabm.4c01600. Epub 2024 Dec 19.

Abstract

Proteins are important biological macromolecules that perform a wide variety of functions in the cell and human body, and can serve as important biomarkers for early diagnosis and prognosis of human diseases as well as monitoring the effectiveness of disease treatment. Hence, sensitive and accurate detection of proteins in human biospecimens is imperative. However, at present, there is no ideal method available for the detection of proteins in clinical samples, many of which are present at ultralow (less than 1 pM) concentrations and in complicated matrices. Herein, we report an ultrasensitive and selective DNA-assisted CRISPR-Cas12a enhanced fluorescent assay (DACEA) for protein detection with detection limits reaching as low as attomolar concentrations. The high assay sensitivity was accomplished through the combined DNA barcode amplification (by using dual-functionalized AuNPs) and CRISPR analysis, while the high selectivity and high resistance to the matrix effects of our method were accomplished via the formation of protein-antibody sandwich structure and the specific recognition of Cas12a (under the guidance of crRNA) toward the designed target ssDNA. Given its ability to accurately and sensitively detect trace amounts of proteins in complicated matrices, the DACEA protein assay platform pioneered in this work has a potential application in routine protein biomarker testing.

摘要

蛋白质是重要的生物大分子,在细胞和人体中发挥着广泛的功能,并且可以作为人类疾病早期诊断和预后的重要生物标志物,以及监测疾病治疗的效果。因此,灵敏且准确地检测人体生物样本中的蛋白质势在必行。然而,目前尚无理想的方法可用于检测临床样本中的蛋白质,其中许多蛋白质以超低(低于1 pM)浓度存在于复杂的基质中。在此,我们报告了一种用于蛋白质检测的超灵敏且选择性的DNA辅助CRISPR-Cas12a增强荧光检测法(DACEA),其检测限低至阿托摩尔浓度。该检测方法的高灵敏度是通过DNA条形码扩增(使用双功能化金纳米颗粒)和CRISPR分析相结合实现的,而我们方法的高选择性和对基质效应的高抗性则是通过形成蛋白质-抗体夹心结构以及Cas12a(在crRNA的引导下)对设计的目标单链DNA的特异性识别来实现的。鉴于其能够准确灵敏地检测复杂基质中的痕量蛋白质,本工作中首创的DACEA蛋白质检测平台在常规蛋白质生物标志物检测中具有潜在应用价值。

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