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Drawing with Iron on a Gel Containing a Supramolecular Siderophore.在含有超分子铁载体的凝胶上用铁作画。
Angew Chem Int Ed Engl. 2019 Dec 16;58(51):18434-18437. doi: 10.1002/anie.201910872. Epub 2019 Nov 4.
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Construction of a cross-layer linked G-octamer conformational control: a stable G-quadruplex in H-bond competitive solvents.构建跨层连接的G-八聚体构象控制:在氢键竞争溶剂中的稳定G-四链体
Chem Sci. 2019 Mar 6;10(15):4192-4199. doi: 10.1039/c9sc00190e. eCollection 2019 Apr 21.
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Crystal Structure of a Tetrameric DNA Fold-Back Quadruplex.四聚体 DNA 回折四链体的晶体结构。
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Developing a Self-Healing Supramolecular Nucleoside Hydrogel Based on Guanosine and Isoguanosine.基于鸟苷和异鸟苷开发一种自修复超分子核苷水凝胶。
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Self-Assembly of a Guanosine Derivative To Form Nanostructures and Transmembrane Channels.核苷衍生物的自组装形成纳米结构和跨膜通道。
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Small-Molecule-Based Self-Assembled Ligands for G-Quadruplex DNA Surface Recognition.用于G-四链体DNA表面识别的小分子自组装配体
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Thermodynamic and Kinetic Stabilities of G-Quadruplexes in Apolar Solvents.非极性溶剂中 G-四链体的热力学和动力学稳定性。
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Controlling molecularity and stability of hydrogen bonded G-quadruplexes by modulating the structure's periphery.通过调节结构外围来控制氢键连接的 G-四链体的分子性和稳定性。
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Well-defined, persistent, chiral phthalocyanine nanoclusters via G-quadruplex assembly.通过G-四链体组装形成明确、持久的手性酞菁纳米团簇。
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Supramolecular gels made from nucleobase, nucleoside and nucleotide analogs.由碱基、核苷和核苷酸类似物制成的超分子凝胶。
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G-八聚体和 G-十六聚体对单价和二价阳离子的反离子选择性。

Reversed Cation Selectivity of G -Octamer and G -Hexadecamer towards Monovalent and Divalent Cations.

机构信息

Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, Tampa, Florida, 33620, United States.

Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai, 200438, P. R. China.

出版信息

Chem Asian J. 2020 Apr 1;15(7):1030-1034. doi: 10.1002/asia.202000016. Epub 2020 Mar 6.

DOI:10.1002/asia.202000016
PMID:32017419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7138703/
Abstract

A reverse-binding-selectivity between monovalent and divalent cations was observed for two different self-assembly G -hexadecamer and G -octamer systems. The dissociation constant between G -quadruplex and monomer was calculated via VT- H NMR experiments. Quantitative energy profiles revealed entropy as the key factor for the weaker binding toward Ba compared with K in the G -octamer system despite stronger ion-dipole interactions. This study is the first direct comparison of the G -quartet binding affinity between mono and divalent cations and will benefit future applications of G-quadruplex-related research. Further competition experiments between the G -octamer and 18-crown-6 with K demonstrated the potential of this G system as a new potassium receptor.

摘要

在两个不同的自组装 G-十六聚体和 G-八聚体系统中观察到单价和二价阳离子之间的反向结合选择性。通过 VT-H NMR 实验计算了 G-四链体与单体之间的离解常数。定量能量曲线揭示了在 G-八聚体系统中,尽管离子偶极相互作用更强,但熵是 Ba 与 K 相比结合较弱的关键因素。这项研究是单和二价阳离子与 G-四联体结合亲和力的首次直接比较,将有益于未来 G-四联体相关研究的应用。进一步用 K 进行的 G-八聚体和 18-冠-6 之间的竞争实验表明,该 G 体系作为新型钾受体具有潜力。