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Real-time quantitation of intracellular polycation/DNA nanocomplex transport: evidence for directed motion

机译:实时定量细胞内聚阳离子/ DNA纳米复合物运输:定向运动的证据

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Multiple particle tracking (MPT) was used to study the mechanism of gene delivery with a non-viral DNA delivery system. Movements of hundreds of individual fluorescent PEI/DNA nanocomplexes were tracked through COS-7 cells and their transport properties were quantified by calculating their mean-square displacements (MSD). Average MSDs of complexes did not change significantly over the first 5 h post-transfection. At a time scale of 10 s, MSD values ranged from 0.21 to 0.57 /spl mu/m/sup 2/, compared to > 0.32 /spl mu/m/sup 2/ for 6 kb-sized naked DNA. Velocities calculated for individual particles showed some moved as fast as 0.26 /spl mu/m/s, while others were almost immobile. Interestingly, 35% of the complexes were transported in a directed fashion 0.5 h after transfection (rather than random diffusion), a phenomenon that could not be detected by other methods such as Fluorescence Recovery After Photobleaching (FRAP). The percentage of cells undergoing directed transport increased to 62 % after 5 h. Studies such as these should allow the systematic optimization of the physicochemical properties of non-viral gene carriers for enhanced gene transfection efficacy.
机译:使用多粒子跟踪(MPT)来研究使用非病毒DNA传递系统进行基因传递的机制。通过COS-7细胞跟踪了数百个单个荧光PEI / DNA纳米复合物的运动,并通过计算其均方位移(MSD)量化了其转运特性。复合物的平均MSD在转染后的最初5小时内没有显着变化。在10 s的时间尺度上,MSD值的范围从0.21到0.57 / spl mu / m / sup 2 /,而对于6 kb大小的裸DNA而言,> 0.32 / spl mu / m / sup 2 /。计算出的单个颗粒的速度显示某些运动速度高达0.26 / spl mu / m / s,而另一些则几乎不动。有趣的是,转染后0.5小时(而不是随机扩散)以定向方式运输了35%的复合物,这种现象无法通过其他方法(如光漂白后的荧光恢复(FRAP))检测到。 5小时后,进行定向运输的细胞百分比增加到62%。诸如此类的研究应允许非病毒基因载体的理化特性的系统优化,以提高基因转染效率。

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