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首页> 外文期刊>ACS nano >Encapsidated Atom-Transfer Radical Polymerization in Qβ Virus-like Nanoparticles
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Encapsidated Atom-Transfer Radical Polymerization in Qβ Virus-like Nanoparticles

机译:Qβ病毒样纳米颗粒中的衣壳化原子转移自由基聚合。

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摘要

Virus-like particles (VLPs) are unique macromolecular structures that hold great promise in biomedical and biomaterial applications. The interior of the 30 nm-diameter Qβ VLP was functionalized by a three-step process: (1) hydrolytic removal of endogenously packaged RNA, (2) covalent attachment of initiator molecules to unnatural amino acid residues located on the interior capsid surface, and (3) atom-transfer radical polymerization of tertiary amine-bearing methacrylate monomers. The resulting polymer-containing particles were moderately expanded in size; however, biotin-derivatized polymer strands were only very weakly accessible to avidin, suggesting that most of the polymer was confined within the protein shell. The polymer-containing particles were also found to exhibit physical and chemical properties characteristic of positively charged nanostructures, including the ability to easily enter mammalian cells and deliver functional small interfering RNA.
机译:病毒样颗粒(VLP)是独特的大分子结构,在生物医学和生物材料应用中具有广阔的前景。直径为30 nm的QβVLP的内部通过三步过程进行功能化:(1)水解去除内源包装的RNA,(2)引发剂分子与位于内部衣壳表面的非天然氨基酸残基共价连接,以及(3)带有叔胺的甲基丙烯酸酯单体的原子转移自由基聚合。所得的含聚合物的颗粒尺寸适度膨胀。然而,生物素衍生的聚合物链对抗生物素蛋白的接触非常弱,这表明大多数聚合物都被限制在蛋白质壳内。还发现含聚合物的颗粒表现出带正电荷的纳米结构的物理和化学特性,包括易于进入哺乳动物细胞并传递功能性小干扰RNA的能力。

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