| Literature DB >> 32017419 |
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.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