清脆的
核酸
化学
数字聚合酶链反应
核酸检测
微流控
计算生物学
核酸定量
DNA
聚合酶链反应
纳米技术
灵敏度(控制系统)
回文
荧光
核酸法
工作流程
实时聚合酶链反应
样品制备
杂交探针
聚合酶
组合化学
检出限
滚动圆复制
核酸热力学
色谱法
寡核苷酸
锁核酸
生物传感器
生物系统
作者
Sheng Li,Shiwen Tang,Wei Xu,Jianhua Zhou,Xiao Li,Jiasi Wang
标识
DOI:10.1021/acs.analchem.5c08178
摘要
Clustered regularly interspaced short palindromic repeat (CRISPR) systems show great promise for next-generation molecular diagnostics due to their programmability and specificity. Amplification-free CRISPR detection has a strong potential for point-of-care (POC) testing, and the digital format of the assay naturally improves the sensitivity of amplification-free CRISPR detection. However, integrating sample preparation, reaction implementation, and signal readout into a streamlined and user-friendly POC workflow remains a major technical challenge. We address this by developing SIMPLE-CRISPR (Sample-to-Result Integrated platform with Magnetic-bead extraction, Polydisperse droplets, Low-complexity operation, and Engineered smartphone readout), an amplification-free CRISPR-Cas12a system for POC diagnostics. Our innovation features functionalized magnetic-bead extraction for the efficient enrichment of low-abundance nucleic acid targets from large-volume samples with minimal loss, vortex-driven polydisperse emulsification for facile digital droplet generation, and smartphone-integrated fluorescence imaging for on-site portable signal detection. This integrated approach significantly improves sensitivity compared to bulk CRISPR, removes the need for amplification and complex microfluidics, and provides sample-to-result functionality for POC environments. Clinical validation for human papillomavirus type 18 (HPV18) detection confirmed that the assay achieved diagnostic performance consistent with quantitative real-time polymerase chain reaction (qRT-PCR), demonstrating its great potential for accessible POC nucleic acid diagnostics.
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