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本文引用的文献

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Clustered Regularly Interspaced Short Palindromic Repeats/Cas9-Mediated Lateral Flow Nucleic Acid Assay.丛集规律间隔短回文重复序列/ Cas9 介导的侧向流动核酸检测。
ACS Nano. 2020 Feb 25;14(2):2497-2508. doi: 10.1021/acsnano.0c00022. Epub 2020 Feb 14.
2
Cas12a-Based On-Site and Rapid Nucleic Acid Detection of African Swine Fever.基于Cas12a的非洲猪瘟现场快速核酸检测
Front Microbiol. 2019 Dec 10;10:2830. doi: 10.3389/fmicb.2019.02830. eCollection 2019.
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Cas12aVDet: A CRISPR/Cas12a-Based Platform for Rapid and Visual Nucleic Acid Detection.Cas12aVDet:一种基于 CRISPR/Cas12a 的快速可视化核酸检测平台。
Anal Chem. 2019 Oct 1;91(19):12156-12161. doi: 10.1021/acs.analchem.9b01526. Epub 2019 Sep 11.
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CRISPR/Cas Multiplexed Biosensing: A Challenge or an Insurmountable Obstacle?CRISPR/Cas 多重生物传感:挑战还是无法逾越的障碍?
Trends Biotechnol. 2019 Aug;37(8):792-795. doi: 10.1016/j.tibtech.2019.04.012. Epub 2019 May 29.
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Synergistically enhanced colorimetric molecular detection using smart cup: a case for instrument-free HPV-associated cancer screening.协同增强比色分子检测使用智能杯:一种用于无仪器 HPV 相关癌症筛查的方法。
Theranostics. 2019 Apr 13;9(9):2637-2645. doi: 10.7150/thno.32224. eCollection 2019.
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CRISPR/Cas Systems towards Next-Generation Biosensing.CRISPR/Cas 系统在下一代生物传感中的应用。
Trends Biotechnol. 2019 Jul;37(7):730-743. doi: 10.1016/j.tibtech.2018.12.005. Epub 2019 Jan 14.
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Programmed DNA destruction by miniature CRISPR-Cas14 enzymes.通过微型 CRISPR-Cas14 酶实现程序化 DNA 破坏。
Science. 2018 Nov 16;362(6416):839-842. doi: 10.1126/science.aav4294. Epub 2018 Oct 18.
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Effect of Screening With Primary Cervical HPV Testing vs Cytology Testing on High-grade Cervical Intraepithelial Neoplasia at 48 Months: The HPV FOCAL Randomized Clinical Trial.HPV 焦点随机临床试验:48 个月时,用初级宫颈 HPV 检测与细胞学检测筛查对高级别宫颈上皮内瘤变的影响。
JAMA. 2018 Jul 3;320(1):43-52. doi: 10.1001/jama.2018.7464.
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CRISPR-Cas12a-assisted nucleic acid detection.CRISPR-Cas12a辅助的核酸检测
Cell Discov. 2018 Apr 24;4:20. doi: 10.1038/s41421-018-0028-z. eCollection 2018.
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Field-deployable viral diagnostics using CRISPR-Cas13.现场部署的基于 CRISPR-Cas13 的病毒诊断方法
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用于基于CRISPR-Cas12a的一锅法超灵敏定量分子诊断的动态水相多相反应系统

Dynamic Aqueous Multiphase Reaction System for One-Pot CRISPR-Cas12a-Based Ultrasensitive and Quantitative Molecular Diagnosis.

作者信息

Yin Kun, Ding Xiong, Li Ziyue, Zhao Hui, Cooper Kumarasen, Liu Changchun

机构信息

Department of Biomedical Engineering, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, Connecticut 06030, United States.

Department of Mechanical Engineering, University of Nevada, Las Vegas, Las Vegas, Nevada 89154, United States.

出版信息

Anal Chem. 2020 Jun 16;92(12):8561-8568. doi: 10.1021/acs.analchem.0c01459. Epub 2020 May 22.

DOI:10.1021/acs.analchem.0c01459
PMID:32390420
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7588651/
Abstract

Recently, CRISPR-Cas technology has opened a new era of nucleic acid-based molecular diagnostics. However, current CRISPR-Cas-based nucleic acid biosensing has a lack of the quantitative detection ability and typically requires separate manual operations. Herein, we reported a dynamic aqueous multiphase reaction (DAMR) system for simple, sensitive and quantitative one-pot CRISPR-Cas12a based molecular diagnosis by taking advantage of density difference of sucrose concentration. In the DAMR system, recombinase polymerase amplification (RPA) and CRISPR-Cas12a derived fluorescent detection occurred in spatially separated but connected aqueous phases. Our DAMR system was utilized to quantitatively detect human papillomavirus (HPV) 16 and 18 DNAs with sensitivities of 10 and 100 copies within less than 1 h. Multiplex detection of HPV16/18 in clinical human swab samples were successfully achieved in the DAMR system using 3D-printed microfluidic device. Furthermore, we demonstrated that target DNA in real human plasma samples can be directly amplified and detected in the DAMR system without complicated sample pretreatment. As demonstrated, the DAMR system has shown great potential for development of next-generation point-of-care molecular diagnostics.

摘要

最近,CRISPR-Cas技术开启了基于核酸的分子诊断新时代。然而,目前基于CRISPR-Cas的核酸生物传感缺乏定量检测能力,并且通常需要单独的手动操作。在此,我们报道了一种动态水相多相反应(DAMR)系统,通过利用蔗糖浓度的密度差异,实现了基于CRISPR-Cas12a的简单、灵敏且定量的一锅式分子诊断。在DAMR系统中,重组酶聚合酶扩增(RPA)和CRISPR-Cas12a衍生的荧光检测在空间上分离但相连的水相中发生。我们的DAMR系统用于定量检测人乳头瘤病毒(HPV)16和18 DNA,在不到1小时内灵敏度达到10和100拷贝。使用3D打印微流控装置在DAMR系统中成功实现了临床人拭子样本中HPV16/18的多重检测。此外,我们证明了在DAMR系统中,真实人血浆样本中的目标DNA无需复杂的样本预处理即可直接扩增和检测。如所示,DAMR系统在下一代即时分子诊断的开发中显示出巨大潜力。