Cas9
核糖核蛋白
基因组编辑
内体
清脆的
细胞内
化学
细胞生物学
生物物理学
生物化学
生物
核糖核酸
基因
作者
Toru Taharabaru,Takuya Kihara,Risako Onodera,Tetsuya Kogo,Kenjirou Higashi,Kunikazu Moribe,Teruya Nakamura,Keiichi Motoyama,Taishi Higashi
标识
DOI:10.1016/j.apmt.2022.101488
摘要
Cas9 ribonucleoprotein (Cas9 RNP) is a promising genome editing tool, however its biological utility reuires the development of safe, efficient, and easy-to-use non-viral carriers. Cas9 RNP has a complicated conformation and charge distribution, resulting in low complexation with carriers. In addition, intracellular uptake, endosome escape, release, and nuclear translocation of Cas9 RNP are required. Here, we report the development of polyrotaxane-based supramolecular carriers, aminated polyrotaxanes (amino-PRXs), that efficiently form complexes with Cas9 RNP via their autonomous transforming properties (1st generation; 1 G). Further, the amino groups of amino-PRXs are optimized to provide endosome-escape ability (2 G) via transforming to highly cationic particles in the endosome. Moreover, intracellular degradation properties are provided for Cas9 RNP release (3G–5 G) resulting in released Cas9 RNP becoming localized in the nucleus. Finally, we demonstrate that this optimized amino-PRX (5 G) facilitates highly efficient genome editing both in vitro and in vivo with significant usability, suggesting that amino-PRX (5 G) is a promising platform for the development of non-viral Cas9 RNP carriers.
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