纳米囊
纳米技术
下调和上调
化学
小RNA
基因传递
细胞生物学
串扰
脱氧核酶
抑制器
生物物理学
基因
药物输送
纳米凝胶
细胞凋亡
肿瘤细胞
纳米医学
计算生物学
特洛伊木马
内化
材料科学
遗传增强
癌症研究
基因靶向
微泡
HEK 293细胞
计算机科学
分解代谢
输送系统
纳米颗粒
基因表达
作者
Xiaoqi Tang (12996656),Yihui Chen (446576),Binpan Wang (15410796),Dan Luo (192943),Jue Wang (58890),Yuan He (82781),Liu Feng (8352141),Ying Xu (9172),Shuang Xie (1497583),Ming Chen (115604),Kai Chang (149548)
出处
期刊:
[Figshare (United Kingdom)]
日期:2024-05-16
标识
DOI:10.1021/acsnano.4c04147.s001
摘要
Manipulating the expression of cellular genes through efficient CRISPR/Cas9 delivery is rapidly evolving into a desirable tumor therapeutics. The exposure of CRISPR/Cas9 to a complex external environment poses challenges for conventional delivery carriers in achieving responsive and accurate release. Here, we report a Trojan horse-like nanocapsule for the on-demand delivery of CRISPR/Cas9 in a microRNA-responsive manner, enabling precise tumor therapy. The nanocapsule comprises a nanoassembled, engineered DNAzyme shell encasing a Cas9/sgRNA complex core. The DNAzyme, functioning as a catalytic unit, undergoes a conformational change in the presence of tumor-associated microRNA, followed by activating a positive feedback-driven autonomous catabolic cycle of the nanocapsule shell. This catabolic cycle is accomplished through chain reactions of DNAzyme “cleavage–hybridization–cleavage”, which ensures sensitivity in microRNA recognition and effective release of Cas9/sgRNA. Utilizing this Trojan horse-like nanocapsule, as low as 1.7 pM microRNA-21 can trigger the on-demand release of Cas9/sgRNA, enabling the specific editing of the protumorigenic microRNA coding gene. The resulting upregulation of tumor suppressor genes induces apoptosis in tumor cells, leading to significant inhibition of tumor growth by up to 75.94%. The Trojan horse-like nanocapsule, with superior programmability and biocompatibility, is anticipated to serve as a promising carrier for tailoring responsive gene editing systems, achieving enhanced antitumor specificity and efficacy.
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