Electrochemical gene detection based on supramolecular complex formation by ferrocenyl-β-cyclodextrin and adamantylnaphthalene diimide bound to double stranded DNA

被引:25
|
作者
Sato, S [1 ]
Nojima, T [1 ]
Takenaka, S [1 ]
机构
[1] Kyushu Univ, Fac Engn, Dept Appl Chem, Fukuoka 8128581, Japan
关键词
adamantylnaphthalene diimide; ferrocenyl-beta-cyclodextrin; supramolecular complex; double stranded DNA; electrochemical detection;
D O I
10.1016/j.jorganchem.2004.08.039
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Adamantylnaphthalene diimide 1 was synthesized as a highly selective double stranded DNA (dsDNA) binding reagent. The binding studies with sonicated calf thymus DNA as a model of dsDNA revealed that 1 can bind to dsDNA by the threading mode, where the two adamantyl moieties are located in the major and minor grooves of dsDNA separately and the complex of 1 with DNA duplex was stabilized by capping of the adamantyl moieties of 1 bound to dsDNA by beta-cyclodextrin. The adamantyl moieties of 1 could be incorporated also into the cavity of ferrocenyl-beta-cyclodextrin (Fc-beta-CD), resulting in the formation of a supramolecular complex. When this complex is formed on the DNA probe-immobilized electrode, electrochemical DNA detection was feasible: the electrode hybridized with target DNA gave rise to a current peak corresponding to the ferrocene oxidation upon treatment with 1 and Fc-beta-CD. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:4722 / 4728
页数:7
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