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串联半稳定互补结构域对序列定义 DNA 嵌段共聚物协同效应的研究。

Studies on the Synergistic Effect of Tandem Semi-Stable Complementary Domains on Sequence-Defined DNA Block Copolymers.

机构信息

Engineering Research Center of Advanced Rare Earth Materials (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, China.

State Key Laboratory of Chemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.

出版信息

J Am Chem Soc. 2022 Nov 23;144(46):21267-21277. doi: 10.1021/jacs.2c08930. Epub 2022 Nov 14.

Abstract

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.

摘要

串联半稳定互补结构域在生命中起着重要作用,而这些结构域在核酸分子折叠过程中的作用尚未得到系统研究。在这里,我们通过合成由具有回文序列的 ssDNA 片段和正交的低聚(四乙二醇)(OEG)接头组成的序列定义的 DNA-OEG 共聚物,设计了一个清洁的模型系统。通过分别改变 DNA 单元(6-12nt)和 OEG 接头(Xn=0-4)的长度,我们系统地研究了串联互补结构域的稳定性和连接的柔韧性如何影响组装拓扑结构。结合实验方法和粗粒度分子模拟分析,我们对多种组装构象(主要是单体、二聚体和聚集体)的分布进行了表征。结果都表明,由于协同增强效应,串联半稳定互补结构域倾向于形成同质的封闭圆形二聚体,而不是更大的聚集体,并且每种构象的分布高度依赖于柔韧性。

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