Lateral Distribution of Charged Species along a Polyelectrolyte Probed with a Fluorescence Blob Model

被引:4
|
作者
Keyes-Baig, Christine [1 ]
Mathew, Manoj [1 ]
Duhamel, Jean [1 ]
机构
[1] Univ Waterloo, Dept Chem, Polymer Res Inst, Waterloo Inst Nanotechnol, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
PHOTOINDUCED ELECTRON-TRANSFER; INTERCALATED ETHIDIUM-BROMIDE; SIDE-CHAIN DYNAMICS; COUNTERION CONDENSATION; LIMITING LAWS; LONG-RANGE; DISTANCE DEPENDENCE; LUMINESCENT PROBES; DNA COMPLEXES; VISCOSITY;
D O I
10.1021/ja307352h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The distribution of metal counterions binding onto the oppositely charged surface of a model polyelectrolyte, namely, DNA, was characterized by conducting fluorescence quenching experiments. In these experiments, DNA was used as a molecular ruler to measure the average distance (d(blob)) over which electron transfer takes place between DNA-intercalated ethidium bromide (DNA-EB) and the electrostatically bound divalent metal cations Ni2+ and Cu2+. Analysis of the fluorescence decays of DNA-EB quenched by Cu2+ and Nil with the fluorescence blob model showed that d(blob), was equal to the Debye length (kappa(-1)). This surprisingly simple result considering the overall complexity of the system under study led to the straightforward proposal that counterions bind to a polyelectrolyte by distributing themselves randomly into an array of self-defined subdomains of dimension kappa(-1). In turn, this insight can be utilized to rationalize the complex behavior of polyelectrolytes in aqueous solution.
引用
收藏
页码:16791 / 16797
页数:7
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