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首页> 外文期刊>Biomacromolecules >Bait-and-Switch Supramolecular Strategy To Generate Noncationic RNA-Polymer Complexes for RNA Delivery
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Bait-and-Switch Supramolecular Strategy To Generate Noncationic RNA-Polymer Complexes for RNA Delivery

机译:用于产生RNA递送的非化RNA聚合物复合物的诱饵和切换的超分子策略

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摘要

RNA interference (RNAi) requires the intracellular delivery of RNA molecules to initiate the neutralization of targeted mRNA molecules, inhibiting the expression or translation of the targeted gene. Current polymers and lipids that are used to deliver RNA molecules are generally required to be positively charged, to achieve complexation with RNA and the cellular internalization. However, positive surface charge has been implicated as the reason for toxicity in many of these systems. Herein, we report a novel strategy to generate noncationic RNA-polymer complexes for RNA delivery with low cytotoxicity. We use an in situ electrostatic complexation using a methylated pyridinium group, which is simultaneously removed during the RNA binding step. The resultant complexes demonstrate successful knockdown in preimplantation mammalian embryos, thus providing a new approach for nucleic acid delivery.
机译:RNA干扰(RNAi)需要细胞内递送RNA分子以引发靶向mRNA分子的中和,抑制靶向基因的表达或翻译。 通常需要用于递送RNA分子的电流聚合物和脂质被带正电,以实现与RNA和细胞内化的络合。 然而,正表面电荷涉及许多这些系统中的许多毒性的原因。 在此,我们报告了一种新的策略,以产生具有低细胞毒性的RNA递送的非化性RNA聚合物复合物。 我们使用甲基化吡啶基团的原位静电络合,在RNA结合步骤期间同时除去。 所得复合物在预催化哺乳动物胚胎中表现出成功的敲低,从而为核酸输送提供了一种新方法。

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