| Literature DB >> 34105245 |
Qian Ban1, Peng Yang2, Shih-Jie Chou3, Li Qiao1, Haidong Xia1, Jingjing Xue2, Fang Wang4, Xiaobin Xu5,6, Na Sun2, Ryan Y Zhang2, Ceng Zhang2, Athena Lee2, Wenfei Liu5, Ting-Yi Lin3, Yu-Ling Ko3, Petar Antovski2, Xinyue Zhang2, Shih-Hwa Chiou3, Chin-Fa Lee7, Wenqiao Hui8, Dahai Liu9, Steven J Jonas10, Paul S Weiss5, Hsian-Rong Tseng2.
Abstract
The clustered regularly interspaced short palindromic repeats (CRISPR)-associated protein 9 (CRISPR/Cas9) is an efficient and precise gene-editing technology that offers a versatile solution for establishing treatments directed at genetic diseases. Currently, CRISPR/Cas9 delivery into cells relies primarily on viral vectors, which suffer from limitations in packaging capacity and safety concerns. These issues with a nonviral delivery strategy are addressed, where Cas9•sgRNA ribonucleoprotein (RNP) complexes can be encapsulated into supramolecular nanoparticles (SMNP) to form RNP⊂SMNPs, which can then be delivered into targeted cells via supramolecular nanosubstrate-mediated delivery. Utilizing the U87 glioblastoma cell line as a model system, a variety of parameters for cellular-uptake of the RNP-laden nanoparticles are examined. Dose- and time-dependent CRISPR/Cas9-mediated gene disruption is further examined in a green fluorescent protein (GFP)-expressing U87 cell line (GFP-U87). The utility of an optimized SMNP formulation in co-delivering Cas9 protein and two sgRNAs that target deletion of exons 45-55 (708 kb) of the dystrophin gene is demonstrated. Mutations in this region lead to Duchenne muscular dystrophy, a severe genetic muscle wasting disease. Efficient delivery of these gene deletion cargoes is observed in a human cardiomyocyte cell line (AC16), induced pluripotent stem cells, and mesenchymal stem cells.Entities:
Keywords: CRISPR/Cas9; Duchenne muscular dystrophy; gene editing; nanosubstrate-mediated delivery; supramolecular nanoparticles
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Year: 2021 PMID: 34105245 PMCID: PMC8282741 DOI: 10.1002/smll.202100546
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 15.153