生物传感器
核酸
变构调节
纳米技术
计算生物学
适体
合成生物学
小分子
核酸检测
DNA
钥匙(锁)
化学
计算机科学
反式激活crRNA
序列(生物学)
DNA纳米技术
蛋白质工程
分子识别
作者
Juan Li,Tong Shao,Xin-Jiao Cao,Ya-Xin Wang,De-Ming Kong
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2026-01-01
卷期号:26 (4): 917-929
摘要
-cleavage activity of CRISPR/Cas12a could be triggered through leveraging proximity-based TSDR in response to target binding. The proposed sensor achieved sensitive and specific detection of various targets, including nucleic acids (HPV-16), small molecules (kanamycin), and enzymes (uracil-DNA glycosylase). Furthermore, by integrating lateral flow assay technology, this CRISPR/Cas12a-based system enabled point-of-care testing (POCT) for the detection of multiple target types. This approach can overcome the sequence-specific limitations, thereby improving the versatility of CRISPR/Cas12a sensors for extending more target types detection. We anticipate this innovative technology will serve as a flexible and accessible sensing platform, facilitating rapid diagnosis in the field of POCT and enabling its broader application across diverse biotechnological domains.
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