Kashida Hiromu, Nishikawa Keiji, Shi Wenjing, Miyagawa Toshiki, Yamashita Hayato, Abe Masayuki, Asanuma Hiroyuki
Department of Biomolecular Engineering, Graduate School of Engineering, Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan
Graduate School of Engineering Science, Osaka University 1-3, Machikaneyama Toyonaka Osaka 560-8531 Japan.
Chem Sci. 2021 Jan 12;12(5):1656-1660. doi: 10.1039/d0sc05245k.
Herein we report an amplification system of helical excess triggered by nucleic acid hybridization for the first time. It is usually impossible to prepare achiral nanostructures composed of nucleic acids because of their intrinsic chirality. We used serinol nucleic acid (SNA) oligomers for the preparation of achiral nanowires because SNA oligomers with symmetrical sequences are achiral. Nanowire formation was confirmed by atomic force microscopy and size exclusion chromatography. When a chiral nucleic acid with a sequence complementary to SNA was added to the nanostructure, helicity was induced and a strong circular dichroism signal was observed. The SNA nanowire could amplify the helicity of chiral nucleic acids through nucleobase stacks. The SNA nanostructures have potential for use as platforms to detect chiral biomolecules under aqueous conditions because SNA can be readily functionalized and is water-soluble.
在此,我们首次报道了一种由核酸杂交引发的螺旋度放大系统。由于核酸固有的手性,通常不可能制备由核酸组成的非手性纳米结构。我们使用丝氨醇核酸(SNA)寡聚物来制备非手性纳米线,因为具有对称序列的SNA寡聚物是非手性的。通过原子力显微镜和尺寸排阻色谱法确认了纳米线的形成。当将具有与SNA互补序列的手性核酸添加到纳米结构中时,会诱导螺旋度并观察到强烈的圆二色性信号。SNA纳米线可以通过核碱基堆积放大手性核酸的螺旋度。SNA纳米结构有潜力用作在水性条件下检测手性生物分子的平台,因为SNA易于功能化且可溶于水。