核糖核蛋白
Cas9
化学
细胞内
清脆的
胞浆
生物化学
基因传递
细胞生物学
基因
遗传增强
生物
核糖核酸
酶
作者
Echuan Tan,Tao Wan,Chunlei Yu,Qianqian Fan,Wenbang Liu,Hong Chang,Jia Lv,Hui Wang,Dali Li,Ping Yuan,Yiyun Cheng
出处
期刊:Nano Today
[Elsevier]
日期:2022-10-01
卷期号:46: 101617-101617
被引量:17
标识
DOI:10.1016/j.nantod.2022.101617
摘要
Protein therapeutics have emerged as a rapidly growing class of medicine in recent years due to the high potency and specificity. However, protein drugs acting on intracellular targets are currently unavailable due to their membrane impermeability. There is a great demand to develop efficient carriers for intracellular protein delivery. Here, we reported a reactive oxygen species responsive material based on biodegradable polypeptide for this purpose. Boronate moieties were decorated on polypeptides via a p-hydroxybenzylcarbamate self-immolative spacer. The modified polypeptide could catch cargo proteins via ionic interaction and nitrogen/boronate coordination to form uniform nanoparticles, and efficiently release the bound proteins under hydrogen peroxide (H2O2) through the oxidation of boronate ligands. The lead polymer efficiently delivered diverse cargo proteins enter living cells and retained their protein activity. In addition, it efficiently transported Cas9 ribonucleoprotein (RNP) into cells for CRISPR/Cas9 gene editing and achieved liver repair against acetaminophen (APAP)-induced liver injury in mice. The results provided a facile strategy to construct efficient, responsive and biodegradable polymers for cytosolic protein delivery.
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