Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, United States.
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
ACS Appl Mater Interfaces. 2020 Aug 26;12(34):37851-37861. doi: 10.1021/acsami.0c07609. Epub 2020 Aug 17.
DNA-nanoparticle (NP) conjugates have been used to knockdown gene expression transiently and effectively, making them desirable tools for gene regulation therapy. Because DNA-NPs are constitutively active and are rapidly taken up by most cell types, they offer limited control in terms of tissue or cell type specificity. To take a step toward solving this issue, we incorporate toehold-mediated strand exchange, a versatile molecular programming modality, to switch the DNA-NPs from an inactive state to an active state in the presence of a specific RNA input. Because many transcripts are unique to cell subtype or disease state, this approach could one day lead to responsive nucleic acid therapeutics with enhanced specificity. As a proof of concept, we designed conditional deoxyribozyme-nanoparticles (conditional DzNPs) that knockdown tumor necrosis factor α (TNFα) mRNA upon miR-33 triggering. We demonstrate toehold-mediated strand exchange and restoration of TNFα DNAzyme activity in the presence of miR-33 trigger, with optimization of the preparation, configuration, and toehold length of conditional DzNPs. Our results indicate specific and strong ON/OFF response of conditional DzNPs to the miR-33 trigger in buffer. Furthermore, we demonstrate endogenous miR-33-triggered knockdown of TNFα mRNA in mouse macrophages, implying the potential of conditional gene regulation applications using these DzNPs.
DNA-纳米颗粒 (NP) 缀合物已被用于瞬时有效地敲低基因表达,使其成为基因调控治疗的理想工具。由于 DNA-NPs 持续活跃并被大多数细胞类型快速摄取,因此它们在组织或细胞类型特异性方面的控制能力有限。为了解决这个问题,我们引入了引发链交换的分子编程模式,这是一种多功能的分子编程模式,可在存在特定 RNA 输入的情况下将 DNA-NPs 从非活性状态切换到活性状态。由于许多转录物是细胞亚型或疾病状态所特有的,因此这种方法有朝一日可能会导致具有增强特异性的响应性核酸疗法。作为概念验证,我们设计了条件脱氧核酶纳米颗粒 (conditional DzNP),在 miR-33 触发时可降低肿瘤坏死因子 α (TNFα) mRNA 的表达。我们证明了在 miR-33 触发存在的情况下引发链交换和 TNFα DNA 酶活性的恢复,优化了 conditional DzNP 的制备、配置和引发物长度。我们的结果表明 conditional DzNP 对缓冲液中 miR-33 触发具有特异性和强的 ON/OFF 响应。此外,我们证明了内源性 miR-33 触发的 TNFα mRNA 在小鼠巨噬细胞中的敲低,这意味着使用这些 DzNP 进行条件基因调控应用的潜力。