Spatial and Temporal Control of CRISPR-Cas9-Mediated Gene Editing Delivered via a Light-Triggered Liposome System.
Yagiz Alp AksoyBiyao YangWenjie ChenTzongtyng HungRhiannon P KuchelNathan W ZammitShane T GreyEwa M GoldysWei DengPublished in: ACS applied materials & interfaces (2020)
The CRISPR-Cas9 and related systems offer a unique genome-editing tool allowing facile and efficient introduction of heritable and locus-specific sequence modifications in the genome. Despite its molecular precision, temporal and spatial control of gene editing with the CRISPR-Cas9 system is very limited. We developed a light-sensitive liposome delivery system that offers a high degree of spatial and temporal control of gene editing with the CRISPR-Cas9 system. We demonstrated its efficient protein release by respectively assessing the targeted knockout of the eGFP gene in human HEK293/GFP cells and the TNFAIP3 gene in TNFα-induced HEK293 cells. We further validated our results at a single-cell resolution using an in vivo eGFP reporter system in zebrafish (77% knockout). These findings indicate that light-triggered liposomes may have new options for precise control of CRISPR-Cas9 release and editing.
Keyphrases
- crispr cas
- genome editing
- induced apoptosis
- cell cycle arrest
- single cell
- genome wide
- endothelial cells
- copy number
- rheumatoid arthritis
- drug delivery
- high glucose
- endoplasmic reticulum stress
- dna methylation
- single molecule
- amino acid
- rna seq
- quantum dots
- oxidative stress
- gold nanoparticles
- signaling pathway
- small molecule
- genome wide analysis