清脆的
核酸检测
计算机科学
软件可移植性
纳米技术
基因组编辑
杠杆(统计)
计算生物学
风险分析(工程)
数据科学
核酸
系统工程
工程类
生物
人工智能
材料科学
医学
基因
生物化学
程序设计语言
作者
Stefano Del Giovane,Neda Bagheri,Andrea C. Di Pede,Alejandro Chamorro-García,Simona Ranallo,Davide Migliorelli,Loïc Burr,Samantha Paoletti,Hatice Altug,Alessandro Porchetta
标识
DOI:10.1016/j.trac.2024.117594
摘要
The precision and versatility of CRISPR-based techniques, combined with the advantages of nucleic acid-based nanotechnology, hold great promise in transforming the landscape of molecular diagnostics. While significant progress has been made, current CRISPR-based platforms primarly focus on nucleic acid detection. To expand the applicability and fully leverage the advantages offered by CRISPR-based diagnostics, ongoing efforts explore molecular strategies to develop CRISPR sensors capable of detecting a diverse range of analytes beyond nucleic acids. In addition, challenges still persist in the adaptation of CRISPR platforms for point-of-care (POC) applications, involving concerns such as portability and automation, as well as the complexities associated with multiplexing. Here, we provide a detailed classification and comprehensive discussion of molecular strategies facilitating the conversion of non-nucleic acid target binding into CRISPR-powered outputs with an emphasis on their corresponding design principles. Furthermore, the second part of the review outlines current challenges and potential solutions for seamlessly integrating these strategies into user-friendly platforms and rapid tests specifically tailored for point-of-care (POC).
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