脂质体原细胞组装中腺苷触发的动态和瞬态适配体网络

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yu Ouyang, Yang Sung Sohn, Xinghua Chen, Rachel Nechushtai, Eli Pikarsky, Fan Xia, Fujian Huang, Itamar Willner
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引用次数: 0

摘要

基于核酸的瞬态耗散反应电路和本构动态网络的发展作为一种模拟天然动态反应电路的手段引起了人们越来越多的兴趣。报道了近年来应用酶、DNAzymes或光作为催化剂控制DNA网络和电路的瞬时耗散功能的研究进展。此外,在原始细胞集合中的动态网络的集成和潜在应用的识别是具有挑战性的目标。在这里,我们介绍了腺苷(AD)适体亚基复合物与腺苷脱氨酶(ADA)偶联,作为驱动瞬态变构AD稳定DNAzyme电路或耗散AD稳定的结构动态网络的通用识别/催化框架。此外,AD/ ada驱动的瞬态框架作为原始细胞模型集成到脂质体组装中。功能化脂质体携带变质atp稳定的DNAzymes切割EGR-1 mRNA,与MCF-7乳腺癌细胞融合,证明有效的基因治疗和癌细胞的选择性凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Adenosine-Triggered Dynamic and Transient Aptamer-Based Networks Integrated in Liposome Protocell Assemblies

Adenosine-Triggered Dynamic and Transient Aptamer-Based Networks Integrated in Liposome Protocell Assemblies
The development of transient dissipative nucleic-acid–based reaction circuits and constitutional dynamic networks attracts growing interest as a means of emulating native dynamic reaction circuits. Recent efforts applying enzymes, DNAzymes, or light as catalysts controlling the transient, dissipative functions of DNA networks and circuits were reported. Moreover, the integration of the dynamic networks in protocell assemblies and the identification of potential applications are challenging objectives. Here, we introduce the adenosine (AD) aptamer subunit complex coupled with adenosine deaminase (ADA) as a versatile recognition/catalytic framework for driving transient allosterically AD-stabilized DNAzyme circuits or dissipative AD-stabilized constitutional dynamic networks. In addition, the AD/ADA-driven transient frameworks are integrated into liposome assemblies as protocell models. Functionalized liposomes carrying allosterically ATP-stabilized DNAzymes cleaving EGR-1 mRNA are fused with MCF-7 breast cancer cells, demonstrating effective gene therapy and selective apoptosis of cancer cells.
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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