在四面体 DNA 框架上涂覆内溶酶体肽,提高稳定性和细胞输送能力

Jinjun He , Xiang Ji , Zihui Xu , Wei He , Yan Zhao , Lele Sun , Lan Ma
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引用次数: 0

摘要

DNA 纳米结构已成为前景广阔的药物输送载体。然而,稳定性低、细胞吸收效率差以及易被溶酶体降解等挑战仍然阻碍着它们的治疗潜力。在本研究中,我们展示了通过静电相互作用将内溶酶体肽 L17E 包覆在四面体 DNA 框架(TDF)上,以解决这些问题。我们的研究结果表明,L17E包被大大增强了四面体DNA框架的稳定性,并提高了它们通过内吞和大吞噬作用被RAW264.7细胞摄取的效率。此外,L17E包衣还能使TDFs在内质体中高效释放。最后,我们利用涂有 L17E 的 TDF 来递送成骨生长肽,并证明了它在体外和体内抑制牙周炎方面的潜在应用。这种简单易行、成本效益高的策略有望推动 DNA 纳米结构的生物医学应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coating tetrahedral DNA framework with endosomolytic peptides for improved stability and cytosolic delivery

DNA nanostructures have emerged as promising carriers for drug delivery. However, challenges such as low stability, poor cellular uptake efficiency, and vulnerability to lysosomal degradation still hinder their therapeutic potential. In this study, we demonstrate the coating of tetrahedral DNA frameworks (TDF) with the endosomolytic peptide L17E through electrostatic interactions to address these issues. Our findings highlight that L17E coating substantially enhances the stability of TDFs and improves their uptake efficiency into RAW264.7 cells through endocytosis and macropinocytosis. Moreover, L17E coating enables efficient endosomal release of TDFs. Finally, we employed L17E-coated TDF to deliver osteogenic growth peptide and demonstrated its potential applications in inhibiting periodontitis both in vitro and in vivo. This straightforward and cost-effective strategy holds promise for advancing the biomedical applications of DNA nanostructures.

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