Oligonucleotide stabilized silver nanoclusters as fluorescence probe for drug-DNA interaction investigation

被引:50
作者
Yuan, Jipei [1 ]
Guo, Weiwei [1 ]
Wang, Erkang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescence; Silver nanoclusters; Quenching; Drug-DNA interaction; SEQUENCE SPECIFICITY; AG NANOCLUSTERS; HOECHST; 33258; BINDING; QUINACRINE; DAUNOMYCIN; DAUNORUBICIN; MITOXANTRONE; AFM;
D O I
10.1016/j.aca.2011.08.043
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, oligonucleotide stabilized silver nanoclusters as novel fluorescent probes were successfully utilized for the drug-DNA interaction study. Silver nanoclusters were proved to be sensitive probes for the drugs investigated (including of two kinds of intercalators, daunorubicin and quinacrine, as well as a non-intercalating binder bisBenzimide H 33258), as the detection limits at 10(-8) mol L-1 level of studied drugs can be achieved. The interactions of drugs and calf thymus DNA were investigated using non-linear fit analysis, and the binding constants as well as binding site sizes were obtained. As biocompatible materials, silver nanoclusters are promising in the chemical especially biochemical analysis fields. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:338 / 342
页数:5
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