Colloid Au-enhanced DNA immobilization for the electrochemical detection of sequence-specific DNA

被引:209
作者
Cai, H [1 ]
Xu, C [1 ]
He, PG [1 ]
Fang, YZ [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai 200062, Peoples R China
基金
中国国家自然科学基金;
关键词
colloidal Au; DNA immobilization; electrochemical DNA biosensor; detection limit;
D O I
10.1016/S0022-0728(01)00548-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We use colloidal An to enhance the DNA immobilization amount on a g-Old electrode and ultimately lower the detection limit of our electrochemical DNA biosensor. Self-assembly of approximately 16-nm diameter colloidal Au onto a cysteamine modified gold electrode resulted in an easier attachment of an oligonucleotide with a mercaptohexyl group at the 5 ' -phosphate end, and therefore an increased capacity for nucleic acid detection. Quantitative results showed that the surface densities of oligonucleotides on the Au colloid modified gold electrode were approximately (1-4) x 10(14) molecules cm(-2). Hybridization was induced by exposure of the ssDNA-containing gold electrode to ferrocenecarboxaldehyde labeled complementary ssDNA in solution. The detection limit is 5 x 10(-10) mol 1(-1) of complementary ssDNA, which is much lower than our previous electrochemical DNA biosensors. The Au nanoparticle films on the An electrode provide a novel means for ssDNA immobilization and sequence-specific DNA detection. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:78 / 85
页数:8
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