Self-assembly of large RNA structures: learning from DNA nanotechnology

J. M. Stewart, Elisa Franco
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引用次数: 4

Abstract

Abstract Nucleic acid nanotechnology offers many methods to build self-assembled structures using RNA and DNA. These scaffolds are valuable in multiple applications, such as sensing, drug delivery and nanofabrication. Although RNA and DNA are similar molecules, they also have unique chemical and structural properties. RNA is generally less stable than DNA, but it folds into a variety of tertiary motifs that can be used to produce complex and functional nanostructures. Another advantage of using RNA over DNA is its ability to be encoded into genes and to be expressed in vivo. Here we review existing approaches for the self-assembly of RNA and DNA nanostructures and specifically methods to assemble large RNA structures. We describe de novo design approaches used in DNA nanotechnology that can be ported to RNA. Lastly, we discuss some of the challenges yet to be solved to build micron-scale, multi stranded RNA scaffolds.
大RNA结构的自组装:从DNA纳米技术中学习
核酸纳米技术提供了许多利用RNA和DNA构建自组装结构的方法。这些支架在传感、药物传递和纳米制造等多种应用中都很有价值。虽然RNA和DNA是相似的分子,但它们也有独特的化学和结构特性。RNA通常不如DNA稳定,但它可以折叠成各种各样的三级基序,可以用来制造复杂和功能性的纳米结构。与DNA相比,使用RNA的另一个优点是它能够被编码成基因并在体内表达。本文综述了现有的RNA和DNA纳米结构的自组装方法,特别是组装大RNA结构的方法。我们描述了可以移植到RNA的DNA纳米技术中使用的从头设计方法。最后,我们讨论了一些尚未解决的挑战,以建立微米尺度,多链RNA支架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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