核糖核酸
灵活性(工程)
折叠(DSP实现)
纳米技术
计算生物学
生物物理学
计算机科学
化学
生物
材料科学
工程类
生物化学
数学
基因
机械工程
统计
作者
Ewan K.S. McRae,Helena Østergaard Rasmussen,Jianfang Liu,Andreas Bøggild,Michael Nguyen,Néstor Sampedro Vallina,Thomas Boesen,Jan Skov Pedersen,Gang Ren,Cody Geary,Ebbe Sloth Andersen
标识
DOI:10.1038/s41565-023-01321-6
摘要
RNA origami is a method for designing RNA nanostructures that can self-assemble through co-transcriptional folding with applications in nanomedicine and synthetic biology. However, to advance the method further, an improved understanding of RNA structural properties and folding principles is required. Here we use cryogenic electron microscopy to study RNA origami sheets and bundles at sub-nanometre resolution revealing structural parameters of kissing-loop and crossover motifs, which are used to improve designs. In RNA bundle designs, we discover a kinetic folding trap that forms during folding and is only released after 10 h. Exploration of the conformational landscape of several RNA designs reveal the flexibility of helices and structural motifs. Finally, sheets and bundles are combined to construct a multidomain satellite shape, which is characterized by individual-particle cryo-electron tomography to reveal the domain flexibility. Together, the study provides a structural basis for future improvements to the design cycle of genetically encoded RNA nanodevices. RNA nanostructures can be designed to fold during transcription, but the solution structure has remained elusive. Here the authors use cryogenic electron microscopy to determine the structure of a panel of RNA origami shapes and uncover the design and folding principles.
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