期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 116, 期 44, 页码 23821-23825出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp308824j
关键词
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资金
- Slovenian Research Agency [P1-0242, J1-4020]
- COST [MP0802]
- EU FP7 projects EAST-NMR [228461]
- Bio-NMR [261863]
G-quadruplexes are uncanonical DNA structures exhibiting promising characteristics for designing DNA-based nanomaterial and nanodevices. The present NMR study addresses the role of cations, the requiring factor for G-quadruplex formation, in long G-quadruplexes. We investigated d(TG(8)T)(4) and its interactions with (NH4+)-N-15 ions, which provided insights into cation localization within a model of G-quadruplex-based nanowire exhibiting eight stacked G-quartets. All interquartet cavities along the central channel were completely occupied by cations. Determined cation exchange rates demonstrated that (NH4+)-N-15 ions move faster from the binding site between two G-quartets, both composed of all guanine residues in an antiglycesidic conformation with respect to the binding site between all-syn/all-anti G-quartets. These results not only extend previous findings from calculated models of long G-quadruplexes and experimental studies on shorter G-quadruplexes but also establish correlation of kinetics of cation movement with the mode of G-quartet stacking, a potentially valuable relation for understanding G-quadruplex-type specific electronic properties.
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