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聚乙二醇(PEG)拥挤度是决定 pDNA 包装成聚合物胶束方案以增强基因表达的关键因素。

Poly(ethylene glycol) Crowding as Critical Factor To Determine pDNA Packaging Scheme into Polyplex Micelles for Enhanced Gene Expression.

机构信息

Japan Science and Technology Agency, PRESTO , 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan.

Innovation Center of NanoMedicine, Institute of Industrial Promotion - KAWASAKI , 3-25-14 Tonomachi, Kawasaki-ku, Kawasaki 210-0821, Japan.

出版信息

Biomacromolecules. 2017 Jan 9;18(1):36-43. doi: 10.1021/acs.biomac.6b01247. Epub 2016 Dec 19.

Abstract

A critical role of polyethylene glycol (PEG) crowding in the packaging of plasmid DNA (pDNA) into polyplex micelles (PMs) was investigated using a series of PEG-b-poly(l-lysine) (PEG-PLys) block copolymers with varying molecular weights of both PEG and PLys segments. Rod-shaped PMs preferentially formed when the tethered PEG chains covering pDNA in a precondensed state were dense enough to overlap one another (reduced tethering density (RTD) > 1), whereas globular PMs were obtained when they were not overlapped (RTD < 1). These results submitted a scheme that steric repulsive effect of PEG regulated packaging pathways of pDNA either through folding into rod-shape or collapsing into globular depending on whether the PEG chains are overlapped or not. The rod-shaped PMs gave significantly higher gene expression efficacies in a cell-free system compared to the globular PMs, demonstrating the practical relevance of regulating packaging structure of pDNA for developing efficient gene delivery systems.

摘要

聚乙二醇(PEG)拥挤在将质粒 DNA(pDNA)包装成多聚物胶束(PM)中的关键作用,使用一系列具有不同 PEG 和 PLys 段分子量的 PEG-b-聚(L-赖氨酸)(PEG-PLys)嵌段共聚物进行了研究。当覆盖预缩合状态下 pDNA 的束缚 PEG 链足够密集以重叠(束缚密度降低(RTD)> 1)时,优先形成棒状 PM,而当它们不重叠时,则获得球状 PM。这些结果提出了一个方案,即 PEG 的空间排斥效应通过 pDNA 的包装途径进行调节,要么折叠成棒状,要么坍塌成球状,这取决于 PEG 链是否重叠。与球状 PM 相比,在无细胞系统中,棒状 PM 显著提高了基因表达效率,这表明调节 pDNA 的包装结构对于开发有效的基因传递系统具有实际意义。

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