Programmable formation of catalytic RNA triangles and squares by assembling modular RNA enzymes

Hiroki Oi, D. Fujita, Yuki Suzuki, H. Sugiyama, Masayuki Endo, Shigeyoshi Matsumura, Y. Ikawa
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引用次数: 18

Abstract

RNA is a biopolymer that is attractive for constructing nano-scale objects with complex structures. Three-dimensional (3D) structures of naturally occurring RNAs often have modular architectures. The 3D structure of a group I (GI) ribozyme from Tetrahymena has a typical modular architecture, which can be separated into two structural modules (ΔP5 and P5abc). The fully active ribozyme can be reconstructed by assembling the two separately prepared modules through highly specific and strong assembly between ΔP5 ribozyme and P5abc RNA. Such non-covalent assembly of the two modules allows the design of polygonal RNA nano-structures. Through rational redesign of the parent GI ribozyme, we constructed variant GI ribozymes as unit RNAs for polygonal-shaped (closed) oligomers with catalytic activity. Programmed trimerization and tetramerization of the unit RNAs afforded catalytically active nano-sized RNA triangles and squares, the structures of which were directly observed by atomic force microscopy (AFM).
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通过组装模块化RNA酶可编程形成催化RNA三角形和正方形
RNA是一种有吸引力的生物聚合物,用于构建具有复杂结构的纳米级物体。天然rna的三维(3D)结构通常具有模块化结构。四膜虫I族(GI)核酶的三维结构具有典型的模块化结构,可分为两个结构模块(ΔP5和P5abc)。通过ΔP5核酶与P5abc RNA之间的高特异性强组装,将两个单独制备的模块组装在一起,即可重构出完全活性的核酶。这种两个模块的非共价组装允许设计多边形RNA纳米结构。通过对亲本GI核酶的合理重新设计,我们构建了变体GI核酶作为具有催化活性的多边形(封闭)低聚物的单元rna。单元RNA的程序三聚化和四聚化产生具有催化活性的纳米RNA三角形和正方形,其结构可通过原子力显微镜(AFM)直接观察到。
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