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NANOSCOPIC STRUCTURE OF DNA CONDENSED FOR GENE DELIVERY

机译:用于基因传递的缩合DNA的纳米结构

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Scanning force microscopy was used to examine DNA condensates prepared with varying stoichiometries of lipospermine or polyethylenimine in physiological solution. For the first time, individual DNA strands were clearly visualized in incomplete condensates without drying. Using lipospermine at sub-saturating concentrations, discrete nuclei of condensation were observed often surrounded by folded loops of DNA. Similar packing of DNA loops occurred for polyethylenimine-induced condensation. Increasing the amount of the condensing agent led to the progressive coalescence or aggregation of initial condensation nuclei through folding rather than winding the DNA. At over-saturating charge ratios of the cationic lipid or polymer to DNA, condensates had sizes smaller than or equal to those measured previously in electron micrographs. Polyethylenimine condensates were more compact than lipospermine condensates and both produced more homogeneously compacted plasmids when used in a 2-4-fold charge excess. The size and morphology of the condensates may affect their efficiency in transfection.
机译:使用扫描力显微镜检查在生理溶液中用不同化学计量比的脂精胺或聚乙烯亚胺制备的DNA缩合物。第一次,在不完全浓缩的情况下,清晰可见了单个DNA链,而没有干燥。使用亚饱和浓度的脂精胺,观察到冷凝的离散核通常被DNA的折叠环包围。对于聚乙烯亚胺诱导的缩合,发生了类似的DNA环堆积。缩合剂数量的增加导致初始缩合核通过折叠而不是缠绕DNA逐渐进行聚结或聚集。在阳离子脂质或聚合物与DNA的过饱和电荷比下,缩合物的尺寸小于或等于先前在电子显微照片中测得的尺寸。聚乙烯亚胺缩合物比脂精胺缩合物更致密,当以2-4倍电荷过量使用时,两者均产生更均一的致密质粒。冷凝液的大小和形态可能会影响其转染效率。

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