内源性激活的多种dnazyme编码纳米花用于长链非编码RNA的高对比度成像和癌症治疗。

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2025-10-08 DOI:10.1021/acsnano.5c10251
Huimin Yuan, , , Zichen Jiao, , , Tao Wang*, , and , Chun-Yang Zhang*, 
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引用次数: 0

摘要

长链非编码rna (lncRNAs)参与各种生理和病理过程,具有作为诊断生物标志物和治疗靶点的潜力。基于沃森-克里克碱基配对的DNA纳米材料先前已被开发用于诊断指导治疗,但由于非特异性激活和核酸酶易感性,它们受到不希望的信号泄漏和不可控的药物释放的限制。滚动环扩增(RCA)产品可以非典型地自组装成紧凑的DNA纳米花,具有高负载性能和优异的核酸酶抗性,但由于探针的低效整合/释放/激活,它们很少用于细胞内分析。在此,我们设计了内源性酸激活zno封装的RCA纳米花,该纳米花由dna切割DNAzyme (D-DNAzyme)和rna切割DNAzyme (R-DNAzyme)编码,用于lncRNA的高对比度成像,并在活细胞和小鼠中控制癌症治疗。ZnO- rca纳米花内吞进入细胞后,肿瘤细胞的酸性微环境刺激ZnO分解为Zn2+, Zn2+作为DNAzyme辅助因子和治疗性活性氧的产生物。Zn2+激发的d - dnazyme催化的RCA纳米花分离释放失活的R-DNAzyme。在lncRNA存在下,R-DNAzyme恢复活性,以高周转率切割AuNP表面cy5标记的底物探针,特异性敲低survivin基因,导致荧光信号增强,R-DNAzyme介导的基因沉默。值得注意的是,RCA纳米花对核酸酶和酸刺激剥离的内在抗性显著减少了背景信号泄漏,提高了成像对比度。该纳米平台可以精确测量活细胞中的HOTAIR,实时监测小鼠体内的HOTAIR,区分健康和癌变乳腺组织中的HOTAIR水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endogenously Activated Multiple DNAzyme-Encoded Nanoflowers for High-Contrast Imaging of Long Noncoding RNA and Cancer Therapy

Long noncoding RNAs (lncRNAs) are implicated in various physiological and pathological processes with the potential as diagnostic biomarkers and therapeutic targets. Watson–Crick base pairing-based DNA nanomaterials have been developed previously for diagnosis-guided therapy, but they are limited by undesired signal leakage and uncontrollable drug release due to nonspecific activation and nuclease susceptibility. Rolling circle amplification (RCA) products can noncanonically self-assemble into compact DNA nanoflowers with high loading performance and excellent nuclease resistance, but they are scarcely explored for intracellular analysis due to inefficient integration/release/activation of probes. Herein, we design endogenous acid-activatable ZnO-encapsulated RCA nanoflowers encoded by DNA-cleaving DNAzyme (D-DNAzyme) and RNA-cleaving DNAzyme (R-DNAzyme) for high-contrast imaging of lncRNA and controlled cancer therapy in living cells and mice. Upon the endocytosis of ZnO-RCA nanoflowers into the cells, the acidic microenvironment of tumor cells stimulates the decomposition of ZnO into Zn2+ that serves as DNAzyme cofactor and therapeutic reactive oxygen species producer. Zn2+-motivated D-DNAzyme-catalyzed detachment of RCA nanoflowers releases the deactivated R-DNAzyme. In the presence of lncRNA, the activity of R-DNAzyme is restored to cleave Cy5-labeled substrate probes on the AuNP surface with high turnover rate and specifically knocks down survivin gene, resulting in the generation of an enhanced fluorescence signal and R-DNAzyme-mediated gene silencing. Notably, the intrinsic resistance to nucleases and acid-stimulated detachment of RCA nanoflowers dramatically reduce the background signal leakage and improve the imaging contrast. This nanoplatform can accurately measure HOTAIR in living cells, real-time monitor HOTAIR in mice, and distinguish HOTAIR levels in healthy and cancerous breast tissues.

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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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