反式激活crRNA
清脆的
计算生物学
化学
DNA
计算机科学
纳米技术
生物
Cas9
生物化学
材料科学
基因
作者
Zhihao Yao,Wanglu Li,Kaiyu He,Hongmei Wang,Yan Xu,Qun Wu,Liu Wang,Yao Nie
出处
期刊:PubMed
日期:2025-05-08
卷期号:: e2501269-e2501269
标识
DOI:10.1002/advs.202501269
摘要
The CRISPR-Cas12a system has gained significant attention as a rapid nucleic acid diagnostic tool due to its crRNA-guided trans-cleavage activity. Accurately predicting the activity of different targets is significant to facilitate the crRNA availability but remains challenging. In this study, a novel approach is presented that combines molecular dynamics simulations and neural network modeling to predict the trans-cleavage activity. Unlike conventional tools that rely solely on the base sequences, our method integrated sequence features and molecular interaction features of DNA in the CRISPR-Cas12a system, significantly improving prediction accuracy. Through feature importance analysis, key sequence features that influence Cas12a trans-cleavage activity are identified. Additionally, a crRNA-DNA library with over 23 456 feature sequences from representative viruses and bacteria is established, and validated the high predictive accuracy of the model (Pearson's r = 0.9328) by screening crRNAs from reference targets. This study offers new insights into the molecular interactions of Cas12a/crRNA-DNA and provides a reliable framework for optimizing crRNA design, facilitating the application of the CRISPR-Cas12a in rapid nucleic acid diagnostics.
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