Magnetogenetics with Piezo1 Mechanosensitive Ion Channel for CRISPR Gene Editing

被引:9
作者
Shin, Wookjin [1 ]
Jeong, Sumin [1 ,2 ]
Lee, Jung-uk [1 ,2 ]
Jeong, Soo Yeun [1 ]
Shin, Jeonghong [1 ,3 ,4 ]
Kim, Hyongbum Henry [1 ,3 ,4 ]
Cheon, Jinwoo [1 ,5 ,6 ]
Lee, Jae-Hyun [1 ,5 ]
机构
[1] Inst Basic Sci IBS, Ctr Nanomed, Seoul 03722, South Korea
[2] Yonsei Univ, Dept Chem, Seoul 03722, South Korea
[3] Yonsei Univ, Coll Med, Grad Sch Med Sci, Dept Pharmacol,Brain Korea Project 21, Seoul 03722, South Korea
[4] Yonsei Univ, Severance Biomed Sci Inst, Coll Med, Seoul 03722, South Korea
[5] Yonsei Univ, Adv Sci Inst, Grad Program Nano Biomed Engn NanoBME, Seoul 03722, South Korea
[6] Yonsei Univ, Dept Chem, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
Magnetic nanoparticles; torque force; Piezo1 ion channel; gene editing; CRISPR-Cas9; TRANSCRIPTIONAL REGULATION; CALCIUM; GLUCOSE; REMOTE; CELLS;
D O I
10.1021/acs.nanolett.2c02314
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Regulation of genetic activity in single cells and tissues is pivotal to determine key cellular functions in current biomedicine, yet the conventional biochemical activators lack spatiotemporal precision due to the diffusion-mediated slow kinetics and nonselectivity. Here, we describe a magnetogenetic method for target-specific activation of a clustered regularly interspaced short palindromic repeats (CRISPR) system for the regulation of intracellular proteins. We used magnetomechanical force generated by the magnetic nanostructure to activate pre-encoded Piezo1, the mechanosensitive ion channel, on the target cell. The activated Piezo1 further triggers the intracellular Ca(2+ )signaling pathway, inducing the pre-encoded genes to express genes of interest (GOIs), which is Cas9 protein for the CRISPR regulation of the target proteins. We demonstrated that this magnetogenetic CRISPR system successfully edits the target genome for both in vitro and pseudo-in vivo environments, providing a versatile magnetic platform for remote gene editing of animals with various size scales.
引用
收藏
页码:7415 / 7422
页数:8
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