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固相合成和高级 siRNA 及其生物缀合物的自组装。

Solid phase synthesis and self-assembly of higher-order siRNAs and their bioconjugates.

机构信息

Department of Chemistry and Biochemistry, Seton Hall University, South Orange, New Jersey.

Nitto Denko Avecia Inc, Cincinnati, Ohio.

出版信息

Chem Biol Drug Des. 2019 Jun;93(6):999-1010. doi: 10.1111/cbdd.13448. Epub 2018 Dec 23.

Abstract

New methods for the synthesis of higher-order siRNA motifs and their bioconjugates have recently gained widespread attention in the development of new and improved gene therapeutics. Our efforts aim to produce new chemical tools and protocols for the generation of modified siRNAs that screen for important oncogene targets as well as silence their activity for effective gene therapy in cancer models. More specifically, we have developed an efficient solution-phase synthesis for the production of a ribouridine branchpoint synthon that can be effectively incorporated by solid phase synthesis within higher-order RNA structures, including those adopting V-, and Y- and >-< shape RNA templates. Self-assembly of complementary RNA to the template strands produced higher-order siRNA nanostructures that were characterized by a combination of PAGE, DLS, and TEM techniques. In an effort to extend the repertoire of functionally diverse siRNAs, we have also developed solid phase bioconjugation strategies for incorporating bio-active probes such as fatty acid appendages and fluorescent reporters. Taken together, these methods highlight the ability to generate higher-order siRNAs and their bioconjugates for exploring the influence of modified siRNA structure on anti-cancer activity.

摘要

新方法的合成更高阶的 siRNA 基序和它们的生物缀合物最近得到了广泛的关注在新的和改进的基因治疗的发展。我们的努力旨在生产新的化学工具和协议生成修饰的 siRNA 筛选重要癌基因靶标以及沉默其活性的有效基因治疗癌症模型。更具体地说,我们已经开发了一种有效的固相合成生产核糖分支点合成子,可有效掺入更高阶 RNA 结构,包括那些采用 V-、Y-和 >-< 形状 RNA 模板。互补 RNA 模板链的自组装产生了高阶 siRNA 纳米结构,这些结构的特征是 PAGE、DLS 和 TEM 技术的组合。为了扩展功能多样的 siRNA 库,我们还开发了固相生物缀合策略,用于掺入生物活性探针,如脂肪酸附属物和荧光报告器。总之,这些方法突出了生成高阶 siRNA 及其生物缀合物的能力,以探索修饰 siRNA 结构对抗癌活性的影响。

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