Tanaka Takahiro, Matsumura Shigeyoshi, Furuta Hiroyuki, Ikawa Yoshiya
Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, Moto-oka 744, Nishi-ku, Fukuoka, 819-0395, Japan.
Department of Chemistry, Graduate School of Science and Engineering, University of Toyama, Gofuku 3190, Toyama, 930-8555, Japan.
Chembiochem. 2016 Aug 3;17(15):1448-55. doi: 10.1002/cbic.201600190. Epub 2016 Jun 30.
RNA is a promising biomaterial for self-assembly of nano-sized structures with a wide range of applications in nanotechnology and synthetic biology. Several RNA-based nanostructures have been reported, but most are unrelated to intracellular RNA, which possesses modular structures that are sufficiently large and complex to serve as catalysts to promote sophisticated chemical reactions. In this study, we designed dimeric RNA structures based on the Tetrahymena group I ribozyme. The resulting dimeric RNAs (tecto group I ribozyme; tecto-GIRz) exhibit catalytic ability that depended on controlled dimerization, by which a pair of ribozymes can be activated to perform cleavage and splicing reactions of two distinct substrates. Modular redesign of complex RNA structures affords large ribozymes for use as modules in RNA nanotechnology and RNA synthetic biology.
RNA是一种很有前景的生物材料,可用于自组装纳米级结构,在纳米技术和合成生物学中有广泛应用。已经报道了几种基于RNA的纳米结构,但大多数与细胞内RNA无关,细胞内RNA具有足够大且复杂的模块化结构,可作为催化剂促进复杂的化学反应。在本研究中,我们基于嗜热四膜虫I组核酶设计了二聚体RNA结构。所得的二聚体RNA(tecto I组核酶;tecto-GIRz)表现出依赖于可控二聚化的催化能力,通过这种方式,一对核酶可以被激活,以对两种不同的底物进行切割和剪接反应。对复杂RNA结构进行模块化重新设计,可提供大型核酶用作RNA纳米技术和RNA合成生物学中的模块。