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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Gene silencing efficiency of siRNA-PEG conjugates: Effect of PEGylation site and PEG molecular weight
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Gene silencing efficiency of siRNA-PEG conjugates: Effect of PEGylation site and PEG molecular weight

机译:siRNA-PEG偶联物的基因沉默效率:PEG化位点和PEG分子量的影响

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摘要

Small interfering RNA (siRNA) was conjugated with poly(ethylene glycol) (PEG) at four different terminal ends (sense 3', sense 5', antisense 3', and antisense 5') via cleavable disulfide and noncleavable thioether linkages to evaluate their gene silencing efficiencies upon complexation with Lipofectamine?2000. The PEGylation site at the four siRNA termini and PEG molecular weight were not critical factors to significantly affect gene silencing activities. Cleavable siRNA-PEG conjugates showed comparable gene silencing activities to naked siRNA, and exhibited sequence-specific degradation of a target mRNA. Interestingly, noncleavable siRNA-PEG conjugates were processed by Dicer, enabling to exert RNAi effect without showing a target sequence-specific manner. However, only cleavable siRNA-PEG conjugates significantly reduced the extent of INF-α release as compared to noncleavable siRNA-PEG conjugates, suggesting that they can be potentially used for therapeutic siRNA applications.
机译:小干扰RNA(siRNA)通过可裂解的二硫键和不可裂解的硫醚键在四个不同的末端(有义3',有义5',反义3'和反义5')与聚乙二醇(PEG)偶联。与Lipofectamine?2000复合后的基因沉默效率。四个siRNA末端的PEG化位点和PEG分子量不是显着影响基因沉默活性的关键因素。可切割的siRNA-PEG偶联物显示出与裸siRNA相当的基因沉默活性,并显示靶mRNA的序列特异性降解。有趣的是,Dicer对不可切割的siRNA-PEG缀合物进行了处理,从而能够发挥RNAi效应,而无需表现出靶序列特异性方式。然而,与不可切割的siRNA-PEG缀合物相比,仅可切割的siRNA-PEG缀合物显着降低了INF-α释放的程度,表明它们可以潜在地用于治疗性siRNA应用。

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