Interdisciplinary Computing and Complex BioSystems (ICOS), School of Computing Science, Centre for Synthetic Biology and Bioeconomy (CSBB), Centre for Bacterial Cell Biology (CBCB), Newcastle University, Newcastle upon Tyne, NE4 5TG, United Kingdom.
School of Chemistry, Newcastle University, Newcastle upon Tyne, NE1 7RU, United Kingdom.
Sci Rep. 2018 May 3;8(1):6989. doi: 10.1038/s41598-018-25270-6.
RNA presents intringuing roles in many cellular processes and its versatility underpins many different applications in synthetic biology. Nonetheless, RNA origami as a method for nanofabrication is not yet fully explored and the majority of RNA nanostructures are based on natural pre-folded RNA. Here we describe a biologically inert and uniquely addressable RNA origami scaffold that self-assembles into a nanoribbon by seven staple strands. An algorithm is applied to generate a synthetic De Bruijn scaffold sequence that is characterized by the lack of biologically active sites and repetitions larger than a predetermined design parameter. This RNA scaffold and the complementary staples fold in a physiologically compatible isothermal condition. In order to monitor the folding, we designed a new split Broccoli aptamer system. The aptamer is divided into two nonfunctional sequences each of which is integrated into the 5' or 3' end of two staple strands complementary to the RNA scaffold. Using fluorescence measurements and in-gel imaging, we demonstrate that once RNA origami assembly occurs, the split aptamer sequences are brought into close proximity forming the aptamer and turning on the fluorescence. This light-up 'bio-orthogonal' RNA origami provides a prototype that can have potential for in vivo origami applications.
RNA 在许多细胞过程中呈现出有趣的作用,其多功能性为合成生物学中的许多不同应用提供了基础。然而,RNA 折纸作为一种纳米制造方法尚未得到充分探索,并且大多数 RNA 纳米结构基于天然预折叠 RNA。在这里,我们描述了一种生物惰性且独特可寻址的 RNA 折纸支架,它通过 7 个订书钉自组装成纳米带。应用一种算法来生成一种合成的 De Bruijn 支架序列,该序列的特征是缺乏生物活性位点和大于预定设计参数的重复。这种 RNA 支架和互补的订书钉在生理相容的等温条件下折叠。为了监测折叠,我们设计了一种新的分裂西兰花适体系统。适体被分成两个非功能序列,每个序列都集成到与 RNA 支架互补的两条订书钉的 5'或 3'端。通过荧光测量和凝胶成像,我们证明一旦发生 RNA 折纸组装,分裂适体序列就会紧密靠近形成适体并打开荧光。这种点亮的“生物正交”RNA 折纸为体内折纸应用提供了一个原型。