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

Anal Biochem

College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou, 310058, China; Key Laboratory of on Site Processing Equipment for Agricultural Products, Ministry of Agriculture, Hangzhou, 310058, China. Electronic address:

Published: April 2022

AI Article Synopsis

  • Amplification technologies like PCR are commonly used for detecting nucleic acids but have limitations, including the need for complex equipment and risks of false positives due to contamination.
  • The CRISPR/Cas system is emerging as a powerful alternative for nucleic acid detection, utilizing its ability to degrade RNA or DNA quickly, enabling detection without prior amplification.
  • Recent advances in CRISPR-based methods demonstrate comparable sensitivity to traditional amplification methods while addressing challenges in sample preparation, off-target effects, and quantitative detection, suggesting potential for rapid and cost-effective on-site testing.

Article Abstract

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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Source
http://dx.doi.org/10.1016/j.ab.2022.114593DOI Listing

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