设计基于膜锚定 DNA 酶的分子机器,通过定制级联调控增强癌症疗法

Man-Sha Wu, Ze-Rui Zhou, Xiao-Yuan Wang, Xi-Chen Du, Da-Wei Li and Ruo-Can Qian*, 
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引用次数: 0

摘要

基于 DNA 酶的合成结构可实现动态细胞调控。然而,如何设计出一种有效且有针对性的 DNA 酶基结构,以实现可定制的多步骤调控,目前仍有许多研究尚未完成。在此,我们设计了一种基于膜锚定 DNA 酶的分子机器,以实现细胞间和细胞内的动态级联调控,从而实现高效的 T 细胞/癌细胞相互作用以及随后受体介导的癌细胞摄取。我们利用 CD8+ T 细胞和 HeLa 癌细胞作为概念验证,证明所设计的基于 DNA 酶的分子机器可实现定制级联调节,包括:(1)T 细胞和癌细胞之间的特异性识别;(2)对细胞外刺激的特异性响应和荧光感应;以及(3)包括细胞间距离缩短、细胞间通信和抗癌药物细胞内递送在内的级联调节。总之,这项研究工作为基于 DNA 酶的分子机器的定制级联细胞调控提供了一条前景广阔的途径,从而能够通过结合 T 细胞免疫疗法和化疗来加强癌症治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Design of a Membrane-Anchored DNAzyme-Based Molecular Machine for Enhanced Cancer Therapy by Customized Cascade Regulation

Synthetic DNAzyme-based structures enable dynamic cell regulation. However, engineering an effective and targeted DNAzyme-based structure to perform customizable multistep regulation remains largely unexplored. Herein, we designed a membrane-anchored DNAzyme-based molecular machine to implement dynamic inter- and intracellular cascade regulation, which realizes efficient T-cell/cancer cell interactions and subsequent receptor mediated cancer cell uptake. Using CD8+ T-cells and HeLa cancer cells as a proof of concept, we demonstrate that the designed DNAzyme-based molecular machine enables customized cascade regulation including (1) specific recognition between T-cells and cancer cells, (2) specific response and fluorescence sensing upon extracellular stimuli, and (3) cascade regulation including intercellular distance shortening, cell–cell communication, and intracellular delivery of anticancer drugs. Together, this work provides a promising pathway for customized cascade cell regulation based on a DNAzyme-based molecular machine, which enables enhanced cancer therapy by combining T-cell immunotherapy and chemotherapy.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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