胸腺嘧啶
三聚氰胺
氢键
反平行(数学)
碱基对
DNA
分子
复式(建筑)
化学
材料科学
结晶学
有机化学
生物化学
物理
量子力学
磁场
作者
Qian Li,Jiemin Zhao,Longfei Liu,Sagun Jonchhe,Felix J. Rizzuto,Shankar Mandal,Huawei He,Sansen Wei,Hanadi F. Sleiman,Hanbin Mao,Chengde Mao
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2020-07-13
卷期号:19 (9): 1012-1018
被引量:83
标识
DOI:10.1038/s41563-020-0728-2
摘要
The diversity of DNA duplex structures is limited by a binary pair of hydrogen-bonded motifs. Here we show that poly(thymine) self-associates into antiparallel, right-handed duplexes in the presence of melamine, a small molecule that presents a triplicate set of the hydrogen-bonding face of adenine. X-ray crystallography shows that in the complex two poly(thymine) strands wrap around a helical column of melamine, which hydrogen bonds to thymine residues on two of its three faces. The mechanical strength of the thymine-melamine-thymine triplet surpasses that of adenine-thymine base pairs, which enables a sensitive detection of melamine at 3 pM. The poly(thymine)-melamine duplex is orthogonal to native DNA base pairing and can undergo strand displacement without the need for overhangs. Its incorporation into two-dimensional grids and hybrid DNA-small-molecule polymers highlights the poly(thymine)-melamine duplex as an additional tool for DNA nanotechnology.
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