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Molecular logistics using cytocleavable polyrotaxanes for the reactivation of enzymes delivered in living cells

机译:使用可细胞裂解的聚轮烷进行分子物流以重新活化活细胞中传递的酶

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摘要

The intracellular delivery of enzymes is an essential methodology to extend their therapeutic application. Herein, we have developed dissociable supermolecule-enzyme polyelectrolyte complexes based on reduction-cleavable cationic polyrotaxanes (PRXs) for the reactivation of delivered enzymes. These PRXs are characterized by their supramolecular frameworks of a polymeric chain threading into cyclic molecules, which can form polyelectrolyte complexes with anionic enzymes while retaining their three dimensional structure, although their enzymatic activity is reduced. Upon the addition of a reductant, the PRXs dissociate into their constituent molecules and release the enzymes, resulting in a complete recovery of enzymatic activity. Under the intracellular environment, the PRX-based enzyme complexes showed the highest intracellular enzymatic activity and efficient activation of anticancer prodrugs to induce cytotoxic effects in comparison with the non-dissociable complexes and the commercial cell-penetrating peptide-based reagents. Thus, the intracellularly dissociable supermolecules are an attractive system for delivering therapeutic enzymes into living cells.
机译:酶的细胞内递送是扩展其治疗应用的必要方法。在本文中,我们已经开发了基于还原可裂解的阳离子聚轮烷(PRXs)的可解离的超分子酶聚合电解质复合物,用于重新活化所传递的酶。这些PRX的特征在于它们的聚合物链的超分子框架穿入环状分子中,尽管它们的酶活性降低了,但它们可以与阴离子酶形成聚电解质复合物,同时保持其三维结构。加入还原剂后,PRXs分解成它们的组成分子并释放酶,从而完全恢复了酶活性。在细胞内环境下,与不可分离的复合物和可穿透细胞的肽基商业试剂相比,基于PRX的酶复合物显示出最高的细胞内酶活性和抗癌前药的有效活化以诱导细胞毒性作用。因此,细胞内可解离的超分子是用于将治疗性酶递送到活细胞中的有吸引力的系统。

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