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Engineered crRNA for biosensing
DOI:10.1016/j.tibtech.2024.06.006.png)
摘要
En 中文
基于CRISPR/Cas的诊断方法(CRISPR-Dx)面临挑战,包括检测超短核苷酸的困难、预扩增依赖性、交叉污染、原位检测范式的不足,以及检测非核酸靶标的困难。本论坛概述了在工程化CRISPR RNA(crRNA)方面的进展,以解决上述问题,并着重强调了挑战、机遇和未来方向。
期刊
IF:
14.9
论文数:
3.8K
被引数:
2.0W
机构
引用论文
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Foldback-crRNA-Enhanced CRISPR/Cas13a System (FCECas13a) Enables Direct Detection of Ultrashort sncRNA
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Photocontrolled crRNA activation enables robust CRISPR-Cas12a diagnostics光控crRNA激活可实现强大的CRISPR-Cas12a诊断
New design strategies for ultra-specific CRISPR-Cas13a-based RNA detection with single-nucleotide mismatch sensitivity
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Regulating the trans-Cleavage Activity of CRISPR/Cas12a by Using an Elongation-Caged Single-Stranded DNA Activator and the Biosensing Applications
ANALYTICAL CHEMISTRY
IF6.7
A PAM-free CRISPR/Cas12a ultra-specific activation mode based on toehold-mediated strand displacement and branch migration
NUCLEIC ACIDS RESEARCH
IF13.1
Enhancement of trans-cleavage activity of Cas12a with engineered crRNA enables amplified nucleic acid detection
NATURE COMMUNICATIONS
IF15.7
Efficient target cleavage by Type V Cas12a effectors programmed with split CRISPR RNA
NUCLEIC ACIDS RESEARCH
IF13.1

