Beyond the Helix Pitch: Direct Visualization of Native DNA in Aqueous Solution

被引:109
|
作者
Ido, Shinichiro [1 ]
Kimura, Kenjiro [1 ]
Oyabu, Noriaki [1 ]
Kobayashi, Kei [2 ]
Tsukada, Masaru [3 ]
Matsushige, Kazumi [1 ]
Yamada, Hirofumi [1 ]
机构
[1] Kyoto Univ Katsura, Kyoto Univ, Dept Elect Sci & Engn, Nishikyo Ku, Kyoto 6158510, Japan
[2] Kyoto Univ Katsura, Kyoto Univ, Off Soc Acad Collaborat Innovat, Nishikyo Ku, Kyoto 6158510, Japan
[3] Tohoku Univ, WPI AIMR, Aoba Ku, Sendai, Miyagi 9808577, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
double-stranded DNA; frequency modulation atomic force microscopy; nanobioimaging; DNA nanotechnology; molecular self-assembly; ATOMIC-FORCE MICROSCOPY; CANTILEVERS; RESOLUTION; BINDING; LIQUID; TOOL;
D O I
10.1021/nn400071n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The DNA double helix was first elucidated by J.D. Watson and F.H.C. Crick over a half century ago. However, no one could actually "see" the well-known structure ever. Among all real-space observation methods, only atomic force microscopy (AFM) enables us to visualize the biologically active structure of natural DNA in water. However, conventional AFM measurements often caused the structural deformation of DNA because of the strong interaction forces acting on DNA. Moreover, large contact area between the AFM probe and DNA hindered us from imaging sub-molecular-scale features smaller than helical periodicity of DNA. Here, we show the direct observation of native plasmid DNA in water using an ultra-low-noise AFM with the highly sensitive force detection method (frequency modulation AFM: FM-AFM). Our micrographs of DNA vividly exhibited not only overall structure of the B-form double helix in water but also local structures which deviate from the crystallographic structures of DNA without any damage. Moreover, the interaction force area in the FM-AFM was small enough to clearly discern Individual functional groups within DNA. The technique was also applied to explore the synthesized DNA nanostructures toward the current nanobiotechnology. This work will be essential for considering the structure function relationship of biomolecular systems in vivo and for in situ analysis of DNA-based nanodevices.
引用
收藏
页码:1817 / 1822
页数:6
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