A radioactive CRISPR interference system using 89Zr-labeled LbCas12a

被引:0
|
作者
Hwang, Injoo [1 ]
Lee, Jun Young [1 ]
Kim, Tae-Hyun [1 ]
Lee, Eun Ju [2 ]
Kim, Jeeho [3 ]
Park, Hyomin [4 ]
Hur, Min Goo [1 ]
Lee, Sanghwa [5 ]
Park, Jeong-Hoon [1 ,6 ]
机构
[1] Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Daejeon, South Korea
[2] Seoul Natl Univ Hosp, Biomed Res Inst, Seoul, South Korea
[3] Chosun Univ, Sch Med, Dept Pharmacol, Gwangju 501759, South Korea
[4] Seoul Natl Univ, Mol Med & Biopharmaceut Sci, Seoul, South Korea
[5] Catholic Univ Korea, Coll Med, Dept Med Life Sci, Seoul, South Korea
[6] Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Accelerator & Radioisotope Dev Team, Jeongeup Si 56212, Jeollabuk Do, South Korea
基金
新加坡国家研究基金会;
关键词
LbCas12a; Radiolabeled CRISPR; Radiolabeled therapy; CRISPR interference; Zirconium-89; THERAPY;
D O I
10.1016/j.jconrel.2023.11.045
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, CRISPR proteins have been recognized as promising candidates for drug development. However, there is still a lack of substances with the appropriate sensitivity and stability for targeted drug delivery systems. 89Zr is a radioactive isotope that emits positrons, allowing real-time in vivo tracking with proven safety. In this study, we confirmed that labeling with 89Zr did not compromise the functionality of CRISPR proteins during in vivo behavioral imaging. Furthermore, we demonstrated the therapeutic efficacy of the CRISPR interference system in a mouse model of liver fibrosis, highlighting the theragnostic potential of isotope-labeled CRISPR proteins. The findings of this research could contribute to various aspects of ongoing clinical studies exploring the in vivo applications of CRISPR proteins.
引用
收藏
页码:703 / 715
页数:13
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