化学
串联
DNA
单体
核酸
序列(生物学)
串联重复
折叠(DSP实现)
共聚物
分子
回文
立体化学
组合化学
拓扑(电路)
聚合物
生物化学
有机化学
清脆的
工程类
基因组
复合材料
电气工程
组合数学
材料科学
基因
数学
作者
Xin Li,Xiaobin Dai,Yufan Pan,Yawei Sun,Bo Yang,Kun Chen,You Wang,Jiang‐Fei Xu,Yuanchen Dong,Yuhe Renee Yang,Li‐Tang Yan,Dongsheng Liu
摘要
Tandem semi-stable complementary domains play an important role in life, while the role of these domains in the folding process of nucleic acid molecules has not been systematically studied. Here, we designed a clean model system by synthesizing sequence-defined DNA-OEG copolymers composed of ssDNA fragments with palindromic sequences and orthogonal oligo(tetraethylene glycol) (OEG) linkers. By altering the lengths of DNA units (6-12 nt) and OEG linkers (Xn = 0-4) separately, we systematically studied how stabilities of tandem complementary domains and connecting flexibilities affect the assembly topology. Combining experimental methods and coarse-grained molecular simulation analysis, distributions of multiple assembled conformations (mainly monomers, dimers, and clusters) were characterized. Both results indicated that tandem semi-stable complementary domains tend to form homogeneous closed circular dimers instead of larger clusters due to the synergistic enhancement effect, and the distributions of each conformation highly depend on flexibilities.
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