Advances in amplification-free detection of nucleic acid: CRISPR/Cas system as a powerful tool

清脆的 核酸 放大器 核酸检测 多路复用 计算生物学 聚合酶链反应 PCR的应用 多重位移放大 多重聚合酶链反应 生物 生物信息学 生物化学 DNA提取 基因
作者
Siwenjie Qian,Yanju Chen,Xiaoli Xu,Cheng Peng,Xiaofu Wang,Hui Wu,Yang Liu,Xiao‐Ping Zhong,Junfeng Xu,Jian Wu
出处
期刊:Analytical Biochemistry [Elsevier BV]
卷期号:643: 114593-114593 被引量:60
标识
DOI:10.1016/j.ab.2022.114593
摘要

Amplification technologies such as polymerase chain reaction (PCR) play an important role in nucleic acid detection. However, they require bulky and sophisticated thermal cycling instrument, as well as are prone to get false-positive results due to amplicon contamination. Currently, CRISPR/Cas system has become an increasingly popular diagnostic tool for nucleic acid with the discovery of its trans-cleavage activity which can degrade single-stranded DNA or RNA at a very high turnover rate. This inherent signal amplification capability allows CRISPR/Cas system to detect unamplified nucleic acids. Here, we reviewed the recent advances of CRISPR-based amplification-free methods for nucleic acid detection. With the assistance of various signal enhancement strategies, the detection sensitivity could be comparable to that of amplification-based methods. We then presented the pros and cons of these methods. And the subsistent challenges including sample preparation, off-target effect, sequences limit, quantitative and multiplex detection were further discussed in this review. It is probable for CRISPR-powered detection methods to pave the road for rapid, cheap, highly sensitive and specific on-site detection without amplification.
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