细胞内
基因组编辑
Cas9
核糖核蛋白
亚基因组mRNA
纳米载体
核糖核酸
细胞生物学
计算生物学
引导RNA
基因组
材料科学
生物
生物化学
纳米技术
纳米颗粒
基因
作者
Yamin Li,Tao Yang,Yingjie Yu,Nicola Shi,Liu Yang,Zachary Glass,Justin Bolinger,Isaac James Finkel,Wenhan Li,Qiaobing Xu
出处
期刊:Biomaterials
[Elsevier BV]
日期:2018-03-08
卷期号:178: 652-662
被引量:84
标识
DOI:10.1016/j.biomaterials.2018.03.011
摘要
Abstract Protein based therapeutics with high specificities and low off-target effects are used for transient and accurate manipulation of cell functions. However, developing safe and efficient carriers for intracellular delivery of active therapeutic proteins is a long-standing challenge. Here we report a combinatorial library of chalcogen (O, S, Se) containing lipidoid nanoparticles (LNPs) as efficient nanocarriers for intracellular delivery of negatively supercharged Cre recombinase ((-30)GFP-Cre) and anionic Cas9 :single-guide RNA (Cas9:sgRNA) ribonucleoprotein (RNP) for genome editing . The structure-activity relationship between the lipidoids and intracellular protein delivery efficiencies was explored and it was demonstrated that the newly developed LNPs are effective for gene recombination in vivo.
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