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Nanostructures of Cationic Amphophilic Cyclodextrin Complexes with DNA

机译:阳离子两亲性环糊精与DNA的纳米结构。

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摘要

Complexes of cationic amphiphilic cydodextrins heptakis-[2-(ω-amino-oligo(ethylene glycoI))-6-deoxy-6-hexadecylthio]-β-cyclo-dextrin and heptakis[2-(ω-amino-oligo(ethylene glycol))-6-deoxy-6-dodecylthio]-β-cyclodextrin with DNA were examined by small-angle X-ray scattering and dynamic as well as electrophoretic light scattering. The first cyclodextrin forms bilayer vesicles in water, which, in the presence of calf thymus DNA, transform to a multilamellar complex In this complex, the DNA lies between the two polar layers of the cyclodextrin's protonated amino groups in alternation with the lipidic bilayers. The cyclodextrin with shorter lipid chains, in contrast, forms micelles in water, and electrostatic clustering of these about DNA does not affect their intrinsic structure. These results are relevant to the potential of such cyclodextrins in therapeutic gene delivery, showing that their self-assembly modes in isolation influence their complex formation with DNA and possibly their efficiency in promoting cell transfection.
机译:阳离子两亲环糊精庚基-[2-(ω-氨基-寡(乙二醇))-6-脱氧-6-十六烷基硫基]-β-环糊精与庚基[2-(ω-氨基-寡聚(乙二醇) ))用小角X射线散射和动态光以及电泳光散射检查带有DNA的-6-脱氧-6-十二烷基硫基]-β-环糊精。第一个环糊精在水中形成双层囊泡,在小牛胸腺DNA存在的情况下,其转化为多层复合物。在该复合物中,DNA位于环糊精质子化氨基的两个极性层之间,与脂质双层交替排列。相反,具有较短脂质链的环糊精在水中形成胶束,并且这些胶束关于DNA的静电聚集不会影响其内在结构。这些结果与此类环糊精在治疗性基因递送中的潜力有关,表明其孤立的自组装模式影响其与DNA的复合物形成,并可能影响其促进细胞转染的效率。

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