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利用 CRISPR-Cas9 纳米花进行有效的基因组编辑。

Effective Genome Editing Using CRISPR-Cas9 Nanoflowers.

机构信息

Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300350, P. R. China.

出版信息

Adv Healthc Mater. 2022 May;11(10):e2102365. doi: 10.1002/adhm.202102365. Epub 2022 Jan 15.

Abstract

CRISPR-Cas9 as a powerful gene-editing tool has tremendous potential for the treatment of genetic diseases. Herein, a new mesoporous nanoflower (NF)-like delivery nanoplatform termed Cas9-NF is reported by crosslinking Cas9 and polymeric micelles that enables efficient intracellular delivery and controlled release of Cas9 in response to reductive microenvironment in tumor cells. The flower morphology is flexibly tunable by the protein concentration and different types of crosslinkers. Cas9 protein, embedded between polymeric micelles and protected by Cas9-NF, remains stable even under extreme pH conditions. Responsive cleavage of crosslinkers in tumor cells, leads to the traceless release of Cas9 for efficient gene knockout in nucleus. This crosslinked nanoparticle exhibits excellent capability of downregulating oncogene expression and inhibiting tumor growth in a murine tumor model. Taken together, these findings pave a new pathway toward the application of the protein-micelle crosslinked nanoflower for protein delivery, which warrants further investigations for gene regulation and cancer treatment.

摘要

CRISPR-Cas9 作为一种强大的基因编辑工具,在治疗遗传疾病方面具有巨大的潜力。本文报道了一种新型介孔纳米花(NF)样递药纳米平台 Cas9-NF,它通过交联 Cas9 和聚合物胶束来实现,能够在肿瘤细胞的还原微环境中高效实现 Cas9 的细胞内递送和控制释放。通过改变蛋白质浓度和不同类型的交联剂,可灵活调节纳米花的形态。Cas9 蛋白被夹在聚合物胶束之间并受到 Cas9-NF 的保护,即使在极端 pH 条件下也保持稳定。交联剂在肿瘤细胞中的响应性切割导致 Cas9 的无痕迹释放,从而有效地在细胞核中进行基因敲除。这种交联纳米颗粒在小鼠肿瘤模型中表现出优异的下调癌基因表达和抑制肿瘤生长的能力。总之,这些发现为蛋白质-胶束交联纳米花在蛋白质递送上的应用开辟了新的途径,值得进一步研究用于基因调控和癌症治疗。

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