| Literature DB >> 29549971 |
Yamin Li1, Tao Yang2, Yingjie Yu1, Nicola Shi1, Liu Yang1, Zachary Glass1, Justin Bolinger1, Isaac James Finkel1, Wenhan Li1, Qiaobing Xu3.
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.Entities:
Keywords: CRISPR/Cas9; Genome editing; Lipidoids; Protein delivery
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Year: 2018 PMID: 29549971 DOI: 10.1016/j.biomaterials.2018.03.011
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479