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受体靶向多聚物介导的微环与质粒 DNA 的递送。

Minicircle Versus Plasmid DNA Delivery by Receptor-Targeted Polyplexes.

机构信息

1 Pharmaceutical Biotechnology, Center for System-based Drug Research, and Center for NanoScience (CeNS), Ludwig-Maximilians-Universität München , Munich, Germany .

2 Department of Physics, Ludwig-Maximilians-Universität München , Munich, Germany .

出版信息

Hum Gene Ther. 2017 Oct;28(10):862-874. doi: 10.1089/hum.2017.123. Epub 2017 Aug 21.

Abstract

Due to its minimal size and lack of bacterial backbone sequences, minicircle (MC) DNA presents a promising alternative to plasmid DNA (pDNA) for non-viral gene delivery in terms of biosafety and improved gene transfer. Here, luciferase pDNA (pCMV-luc) and analogous MC DNA (MC07.CMV-luc) were formulated into polyplexes with c-Met targeted, PEG-shielded sequence-defined oligoaminoamides, or linear PEI (linPEI) as standard transfection agent. Distinct physicochemical and biological characteristics were observed for polyplexes formed with either pDNA or MC DNA as vectors. The carriers were found to dominate the shape of polyplexes, whereas the DNA type was decisive for the nanoparticle size. c-Met-targeted, tyrosine trimer-containing polyplexes were optimized into compacted rod structures with a size of 65-100 nm for pDNA and 35-40 nm for MC. Notably, these MC polyplexes display a lack of cell cycle dependence of transfection and a ∼200-fold enhanced gene transfer efficiency in c-Met-positive DU145 prostate carcinoma cultures over their tyrosine-free pDNA analogues.

摘要

由于其微小的尺寸和缺乏细菌骨干序列,微环(MC)DNA 在非病毒基因传递方面相对于质粒 DNA(pDNA)具有生物安全性和提高基因转移的优势。在这里,荧光素酶 pDNA(pCMV-luc)和类似的 MC DNA(MC07.CMV-luc)与靶向 c-Met 的聚乙二醇化、序列确定的寡氨基酰胺或线性聚乙烯亚胺(linPEI)形成多聚物,作为标准转染剂。用 pDNA 或 MC DNA 作为载体形成的多聚物表现出明显的物理化学和生物学特性。载体被发现主导多聚物的形状,而 DNA 类型则决定纳米颗粒的大小。含酪氨酸三聚物的 c-Met 靶向多聚物被优化为紧密的棒状结构,pDNA 的大小为 65-100nm,MC 的大小为 35-40nm。值得注意的是,这些 MC 多聚物在 c-Met 阳性的 DU145 前列腺癌细胞培养物中表现出缺乏细胞周期依赖性转染的特点,并且相对于其无酪氨酸的 pDNA 类似物,其基因转移效率提高了约 200 倍。

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