清脆的
Cas9
基因组编辑
计算生物学
核糖核蛋白
质粒
生物
引导RNA
反式激活crRNA
病毒载体
DNA
基因
遗传学
核糖核酸
重组DNA
作者
Hao Cheng,Feng Zhang,Yang Ding
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2021-10-09
卷期号:13 (10): 1649-1649
被引量:61
标识
DOI:10.3390/pharmaceutics13101649
摘要
The clustered regularly interspaced short palindromic repeats (CRISPR)/associated protein 9 (CRISPR/Cas9) systems have emerged as a robust and versatile genome editing platform for gene correction, transcriptional regulation, disease modeling, and nucleic acids imaging. However, the insufficient transfection and off-target risks have seriously hampered the potential biomedical applications of CRISPR/Cas9 technology. Herein, we review the recent progress towards CRISPR/Cas9 system delivery based on viral and non-viral vectors. We summarize the CRISPR/Cas9-inspired clinical trials and analyze the CRISPR/Cas9 delivery technology applied in the trials. The rational-designed non-viral vectors for delivering three typical forms of CRISPR/Cas9 system, including plasmid DNA (pDNA), mRNA, and ribonucleoprotein (RNP, Cas9 protein complexed with gRNA) were highlighted in this review. The vector-derived strategies to tackle the off-target concerns were further discussed. Moreover, we consider the challenges and prospects to realize the clinical potential of CRISPR/Cas9-based genome editing.
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