Structural identification of the novel 3 way-junction motif

D. Jedrzejczyk, A. Chworos
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引用次数: 3

Abstract

Abstract A novel RNA motif was identified based on its sequence by computational structure modeling. The RNA molecule was reported to be a substrate for the structurally specific endoribonuclease, Dicer, which cleaves doublestranded RNA and cuts out 20−25 nucleotide fragments. This enzymatic property was essential for the potential utilization of the motif in the nanoparticle design of further biological experiments. Herein, the protocol for the prediction of the structure of this motif in-silico is presented, starting from its primary sequence and proceeding through secondary and tertiary structure predictions. Applying RNA architectonics, this novel structural motif, 3wj-nRA, was used for rational RNA nanoparticle design. The molecules, which are based on this three-way junction fold, may assemble into more complex, triangular shaped nano-objects. This trimeric nanoparticle containing 3wj-nRA motif can be further utilized for functionalization and application.
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新型三路结基序的结构鉴定
摘要采用计算结构建模的方法,根据RNA基序序列鉴定出一个新的RNA基序。据报道,RNA分子是结构特异性核糖核酸内切酶Dicer的底物,该酶可切割双链RNA并切割20 - 25个核苷酸片段。这种酶的性质对于该基序在进一步生物实验的纳米颗粒设计中的潜在利用是必不可少的。本文提出了该基序的结构预测方案,从其一级序列开始,通过二级和三级结构预测。应用RNA结构学原理,利用这种新型结构基序3wj-nRA进行合理的RNA纳米颗粒设计。基于这种三向结折叠的分子可以组装成更复杂的三角形纳米物体。这种含有3wj-nRA基序的三聚体纳米颗粒可以进一步用于功能化和应用。
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