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聚多肽胶束内 DNA 定量折叠促进基因表达增强。

Enhanced gene expression promoted by the quantized folding of pDNA within polyplex micelles.

机构信息

Department of Materials Engineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.

出版信息

Biomaterials. 2012 Jan;33(1):325-32. doi: 10.1016/j.biomaterials.2011.09.046. Epub 2011 Oct 10.

Abstract

Selective packaging of plasmid DNA (pDNA) into folded rod or collapsed sphere structures in polyplex micelles was demonstrated by modulating the PLys segment length of poly(ethylene glycol)-block- poly(L-lysine) (PEG-PLys) block catiomers used for micelle formation. The two basic packaging structures correlated well to the integrity of double-stranded DNA contained within the micelles. Rod structures formed by the quantized folding mechanism, which results in dissociation of double-stranded DNA only at each fold. Collapsed sphere structures formed by substantial random disruption of the double-stranded DNA structure. Analysis of gene expression in a cell-free transcription/translation system, cultured cells and also skeletal muscle of mice showed that micelles containing pDNA packaged by quantized folding exhibited higher gene expression than naked pDNA and micelles containing collapsed pDNA. These results indicate that controlled packaging of pDNA into an appropriate structure is critical for achieving effective gene expression. Improved gene transfection and expression resulting from the quantized folding of pDNA within polyplex micelles is promising for application in therapeutic gene delivery systems.

摘要

通过调节用于胶束形成的聚乙二醇-聚(L-赖氨酸)(PEG-PLys)嵌段阳离子聚合物中 PLys 段长度,证明了质粒 DNA(pDNA)在多聚物胶束中选择性包装为折叠棒状或塌陷球状结构。这两种基本的包装结构与胶束内双链 DNA 的完整性密切相关。棒状结构是通过定量折叠机制形成的,这导致只有在每个折叠处双链 DNA 才会解离。塌陷球状结构是通过双链 DNA 结构的实质性随机破坏形成的。在无细胞转录/翻译系统、培养细胞以及小鼠骨骼肌中的基因表达分析表明,含有通过定量折叠包装的 pDNA 的胶束比裸露的 pDNA 和含有塌陷 pDNA 的胶束表现出更高的基因表达。这些结果表明,将 pDNA 可控地包装成适当的结构对于实现有效的基因表达至关重要。多聚物胶束内 pDNA 的定量折叠导致的基因转染和表达的改善,为应用于治疗性基因传递系统提供了希望。

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