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硫代磷酸化 DNA 工程化脂质体作为一种通用平台,用于刺激响应型细胞特异性细胞内递药和基因组编辑。

Phosphorothioated DNA Engineered Liposomes as a General Platform for Stimuli-Responsive Cell-Specific Intracellular Delivery and Genome Editing.

机构信息

School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, China.

Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, 201210, China.

出版信息

Angew Chem Int Ed Engl. 2023 Jun 19;62(25):e202303973. doi: 10.1002/anie.202303973. Epub 2023 May 10.

Abstract

Intracellular protein delivery is highly desirable for protein drug-based cell therapy. Established technologies suffer from poor cell-specific cytosolic protein delivery, which hampers the targeting therapy of specific cell populations. A fusogenic liposome system enables cytosolic delivery, but its ability of cell-specific and controllable delivery is quite limited. Inspired by the kinetics of viral fusion, we designed a phosphorothioated DNA coatings-modified fusogenic liposome to mimic the function of viral hemagglutinin. The macromolecular fusion machine docks cargo-loaded liposomes at the membrane of target cells, triggers membrane fusion upon pH or UV light stimuli, and facilitates cytosolic protein delivery. Our results showed efficient cell-targeted delivery of proteins of various sizes and charges, indicating the phosphorothioated DNA plug-in unit on liposomes could be a general strategy for spatial-temporally controllable protein delivery both in vitro and in vivo.

摘要

细胞内蛋白质递送对于基于蛋白质药物的细胞治疗非常理想。已建立的技术存在细胞质蛋白递送效率低的问题,这限制了针对特定细胞群体的靶向治疗。融合脂质体系统能够实现细胞质递送,但它的细胞特异性和可控性递送能力相当有限。受病毒融合动力学的启发,我们设计了一种硫代磷酸化 DNA 涂层修饰的融合脂质体,以模拟病毒血凝素的功能。大分子融合机器将负载货物的脂质体停靠在靶细胞的膜上,在 pH 或紫外光刺激下触发膜融合,并促进细胞质蛋白质的递送。我们的结果表明,各种大小和电荷的蛋白质能够有效地靶向递送到细胞中,这表明脂质体上的硫代磷酸化 DNA 插件单元可以成为体外和体内时空可控蛋白质递送的通用策略。

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