Precise amplification-free detection of highly structured RNA with an enhanced SCas12a assay

The CRISPR/Cas12a system has revolutionized molecular diagnostics, yet the direct detection of RNA, particularly those with complex structures, remains a significant challenge. Here, we present an updated SCas12a system, termed SCas12aV2, which enables precise, amplification-free detection of highly structured RNA molecules. By optimizing the length of scaffold RNA, targeting asymmetric structures, and utilizing dsDNA-ssDNA hybrid activators, we have significantly reduced steric hindrance in the detection system, thereby markedly enhancing both sensitivity and kinetics compared to traditional DNA activators. The SCas12aV2 assay achieves a detection limit of 246 aM for pooled activators and 10 pM for single-site targeting, demonstrating high specificity for single nucleotide polymorphisms (SNPs). It successfully identifies viable bacteria and SARS-CoV-2 infections in clinical samples. The assay is versatile and can be applied to various Cas12a orthologs, including thermostable CtCas12a. This work advances molecular diagnostics by improving the accuracy and efficiency of RNA detection.

Authors

Institutions

Publication Details

Journal
Communications Biology
Published
2025-03-04
DOI
https://doi.org/10.1038/s42003-025-07806-5
Citations
11
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
8.87
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Precise amplification-free detection of highly structured RNA with an enhanced SCas12a assay

Jie Qiao, Wuxiang Mao, Shuqi Jin, Xinping Wang et al.
11 citations
Communications Biology
CRISPR and Genetic Engineering
8.87
article

Precise amplification-free detection of highly structured RNA with an enhanced SCas12a assay

Jie Qiao, Wuxiang Mao, Shuqi Jin, Xinping Wang, Yi Liu, Wenwen Deng, Wenhao Yin, Junqi Zhang, Ruyi He, Qingyuan Jiang
article en
11 citations

Abstract

The CRISPR/Cas12a system has revolutionized molecular diagnostics, yet the direct detection of RNA, particularly those with complex structures, remains a significant challenge. Here, we present an updated SCas12a system, termed SCas12aV2, which enables precise, amplification-free detection of highly structured RNA molecules. By optimizing the length of scaffold RNA, targeting asymmetric structures, and utilizing dsDNA-ssDNA hybrid activators, we have significantly reduced steric hindrance in the detection system, thereby markedly enhancing both sensitivity and kinetics compared to traditional DNA activators. The SCas12aV2 assay achieves a detection limit of 246 aM for pooled activators and 10 pM for single-site targeting, demonstrating high specificity for single nucleotide polymorphisms (SNPs). It successfully identifies viable bacteria and SARS-CoV-2 infections in clinical samples. The assay is versatile and can be applied to various Cas12a orthologs, including thermostable CtCas12a. This work advances molecular diagnostics by improving the accuracy and efficiency of RNA detection.

Communications BiologyVol. 8(1)
Wuhan Polytechnic University (CN), Wuhan University (CN), Zhengzhou University (CN), First Affiliated Hospital of Zhengzhou University (CN), Hubei University (CN)
Openalex Percentile: Top 2%
CRISPR and Genetic Engineering
8.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.