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靶向递送至癌细胞的 DNA 框架包封的天然治疗性蛋白。

Targeted Delivery of DNA Framework-Encapsulated Native Therapeutic Protein into Cancer Cells.

机构信息

Key Laboratory of Luminescence Analysis and Molecular Sensing, Ministry of Education, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

ACS Appl Mater Interfaces. 2020 Dec 9;12(49):54489-54496. doi: 10.1021/acsami.0c17887. Epub 2020 Nov 30.

Abstract

A protein-based therapy is significantly challenged by the successful delivery of native proteins into the targeted cancer cells. We address this challenge here using an all-sealed divalent aptamer tetrahedral DNA framework (asdTDF) delivery platform, in which the protein drug is encapsulated inside the cavity of the framework stoichiometrically a reversible chemical bond. The ligase-assisted seal of the nicks results in highly enhanced TDF stability of the against nuclease digestion to effectively protect the therapeutic protein from degradation. In addition, the divalent aptamer sequences incorporated into the framework favor it with a target-specific and efficient delivery capability. Importantly, upon being readily delivered into the targeted cancer cells, endogenous glutathione can trigger the release of the native therapeutic protein from the TDF in a traceless fashion by cleaving the reversible chemical bond, thereby leading to effective apoptosis of the specific cancer cells.

摘要

基于蛋白质的疗法在将天然蛋白质成功递送到靶向癌细胞方面面临重大挑战。在这里,我们使用全密封的二价适体四面体型 DNA 框架(asdTDF)递药平台来应对这一挑战,其中蛋白质药物通过可逆化学键在框架的腔室内被化学计量地封装。连接酶辅助修复缺口,使 TDF 具有高度增强的稳定性,可有效抵抗核酸酶的消化,从而保护治疗性蛋白质免受降解。此外,整合到框架中的二价适体序列赋予其靶向特异性和高效的递药能力。重要的是,当被递送到靶向癌细胞中时,内源性谷胱甘肽可以通过切割可逆化学键,以无痕迹的方式从 TDF 中释放出天然治疗性蛋白质,从而导致特定癌细胞的有效凋亡。

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