Long-Range Ordered Water Correlations between A-T/C-G Nucleotides

被引:8
|
作者
Luo, Zhonglong [1 ]
Xiao, Hongyan [2 ]
Peng, Xiaochuan [1 ]
Li, Yulong [2 ,3 ]
Zhu, Zhongpeng [4 ]
Tian, Ye [2 ,3 ]
Jiang, Lei [2 ,3 ]
机构
[1] Anhui Univ Technol, Sch Mech Engn, Maanshan 243032, Anhui, Peoples R China
[2] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Bioinspired Mat & Interfacial Sci, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Sch Future Technol, Beijing 100049, Peoples R China
[4] Beihang Univ, Sch Chem, Minist Educ, Key Lab Bioinspired Smart Interfacial Sci & Techn, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
MOLECULE FORCE SPECTROSCOPY; STACKING INTERACTION; DNA; MECHANICS; KINETICS;
D O I
10.1016/j.matt.2020.08.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The interactions between complementary base pairs are crucial to the helical duplex structure of DNA. Although base-base interactions have been widely reported, the study of long-range interactions in the base-pairing processes is still a major challenge in this field. Here, we first study the long-range interactions between the base pairs by atomic force microscopy-based single-molecule force spectroscopy (SMFS). The SMFS results of A-T/C-G imply that there are weak long-range interactions between them, which have a range of 15-25 nm. Raman spectroscopy results imply that these weak interactions can be attributed to multiplex hydrogen bond interaction of ordered water structure between A-T/C-G nucleotides. In addition, the theoretical calculations deduce that the ideal structure of these water molecules exhibits a specific helical structure. Our findings might open up a new understanding of biological assembly processes and provide helpful strategies for bio-nanotechnology.
引用
收藏
页码:794 / 804
页数:11
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