Literature DB >> 32017419

Reversed Cation Selectivity of G8 -Octamer and G16 -Hexadecamer towards Monovalent and Divalent Cations.

Ying He1, Yanbin Zhang2, Lukasz Wojtas1, Novruz G Akhmedov3, Qinhe Pan4, Hao Guo2, Xiaodong Shi1.   

Abstract

A reverse-binding-selectivity between monovalent and divalent cations was observed for two different self-assembly G16 -hexadecamer and G8 -octamer systems. The dissociation constant between G4 -quadruplex and monomer was calculated via VT-1 H NMR experiments. Quantitative energy profiles revealed entropy as the key factor for the weaker binding toward Ba2+ compared with K+ in the G8 -octamer system despite stronger ion-dipole interactions. This study is the first direct comparison of the G4 -quartet binding affinity between mono and divalent cations and will benefit future applications of G-quadruplex-related research. Further competition experiments between the G8 -octamer and 18-crown-6 with K+ demonstrated the potential of this G8 system as a new potassium receptor.
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  G-quadruplex; G-quadruplex dissociation; cation selectivity; entropy; guanosine self-assembly; potassium receptor

Year:  2020        PMID: 32017419      PMCID: PMC7138703          DOI: 10.1002/asia.202000016

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  34 in total

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Journal:  Chem Commun (Camb)       Date:  2016-07-19       Impact factor: 6.222

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  3 in total

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2.  Heterocycle-modified 2'-Deoxyguanosine Nucleolipid Analogs Stabilize Guanosine Gels and Self-assemble to Form Green Fluorescent Gels.

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3.  Construction of Supramolecular Organogel with Circularly Polarized Luminescence by Self-Assembled Guanosine Octamer.

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  3 in total

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