Light-Triggered Genome Editing: Cre Recombinase Mediated Gene Editing with Near-Infrared Light

被引:17
|
作者
Morales, Demosthenes P. [1 ]
Morgan, Erin N. [1 ]
McAdams, Meghan [1 ]
Chron, Amanda B. [1 ]
Shin, Jeong Eun [2 ]
Zasadzinski, Joseph A. [2 ]
Reich, Norbert O. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
gene editing; near-infrared light endosome escape; plasmonics; protein delivery; spatiotemporal control; PLASMONIC NANOPARTICLES; INTRACELLULAR DELIVERY; GOLD NANOSHELLS; EFFICIENT; PROTEINS; PEPTIDES; SIRNA;
D O I
10.1002/smll.201800543
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A light-activated genome editing platform based on the release of enzymes from a plasmonic nanoparticle carrier when exposed to biocompatible near-infrared light pulses is described. The platform relies on the robust affinity of polyhistidine tags to nitrilotriacetic acid in the presence of copper which is attached to double-stranded nucleic acids self-assembled on the gold nanoparticle surface. A protein fusion of the Cre recombinase containing a TAT internalization peptide sequence to achieve endosomal localization is also employed. High-resolution gene knock-in of a red fluorescent reporter is observed using a commercial two-photon microscope. High-throughput irradiation is described to generate useful quantities of edited cells.
引用
收藏
页数:8
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