清脆的
核酸
DNA
计算生物学
寡核苷酸
劈理(地质)
组合化学
化学
生物
纳米技术
分子生物学
生物化学
材料科学
基因
古生物学
断裂(地质)
作者
Rujian Zhao,Yao Xiao,Yidan Tang,Baiyang Lu,Bingling Li
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2024-09-16
标识
DOI:10.1021/acssensors.4c01233
摘要
CRISPR/Cas12a has been widely used in molecular diagnostics due to its excellent trans-cleavage activity. However, conventional reporters, such as F/Q-labeled single-stranded DNA (ssDNA) reporters, enzyme-labeled reporters, and spherical nucleic acid reporters, require complex modification or labeling processes. In this study, we have developed a rapid, universal, and label-free CRISPR/Cas12a-based biomarker detection platform via designing a G-quadruplex (G4) containing a hairpin structure as the reporter. The hairpin loop design of hairpin G4 improves the cleavage efficiency of Cas12a and the signal strength of the G4 binding ligand. Meanwhile, the incorporation of a G4 binding dye (protoporphyrin IX) eliminates the need for complex modifications. The CRISPR-hairpin G4 detection platform is capable of detecting ssDNA, double-stranded DNA, genetic RNAs, and miRNAs. Moreover, this platform achieves label-free detection in clinical samples, demonstrating its practical applicability and efficiency.
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