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Histidylated oligolysines increase the transmembrane passage and the biological activity of antisense oligonucleotides.

机译:组织化的低聚赖氨酸增加反义寡核苷酸的跨膜传递和生物活性。

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摘要

We have designed histidylated oligolysines which increase the uptake, the cytosolic delivery and the nuclear accumulation of antisense oligonucleotides (ODN). Flow cytometry analysis showed a 10-fold enhancement of the ODN uptake in the presence of histidylated oligolysines. The intracellular localizations of fluorescein-labeled ODN and of rhodamine-labeled histidylated oligolysines were investigated by confocal microscopy. Histidylated oligolysines favor the cyto-solic delivery of ODN from endosomes and increase their nuclear accumulation. In contrast, in their absence fluorescent ODN were not observed inside the nucleus but were distributed overwhelmingly within the vesicles in the cytosol. In addition, histidylated oligolysines yielded a more than 20-fold enhancement of the biological activity of antisense ODN towards the inhibition of transient as well as constitutive gene expression. Prevention of endosome lumen acidification using bafilomycin A(1)abolished the effect of histidylated oligolysines, suggesting that protonation of the histidyl residues was involved in the transmembrane passage of ODN.
机译:我们设计了组织化的寡聚赖氨酸,可增加反义寡核苷酸(ODN)的摄取,胞质传递和核积累。流式细胞仪分析显示,在存在组织化的寡聚赖氨酸的情况下,ODN吸收增加了10倍。通过共聚焦显微镜研究了荧光素标记的ODN和若丹明标记的组织化寡聚赖氨酸的细胞内定位。组织化的低聚赖氨酸有利于ODN从内体向细胞的释放,并增加其核积累。相反,在它们不存在的情况下,在细胞核内未观察到荧光ODN,但绝大多数分布在细胞质的囊泡内。另外,组织化寡聚赖氨酸使反义ODN对抑制瞬时以及组成型基因表达的生物学活性提高了20倍以上。预防使用bafilomycin A(1)的内体腔内酸化消除了组织化寡聚赖氨酸的影响,这表明组氨酸残基的质子化参与了ODN的跨膜传递。

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