Selective immobilization of oligonucleotide-modified gold nanoparticles by electrodeposition on screen-printed electrodes

被引:23
|
作者
Moreno, M. [1 ]
Rincon, E. [1 ]
Perez, J. M. [2 ]
Gonzalez, V. M. [3 ]
Domingo, A. [1 ]
Dominguez, E. [4 ]
机构
[1] Univ Alcala, Fac Med, Dept Bioquim & Biol Mol, Madrid 28871, Spain
[2] Bioapter SL, Madrid 28230, Spain
[3] Hosp Ramon & Cajal, Dept Bioquim Invest, E-28034 Madrid, Spain
[4] Univ Alcala, Fac Farm, Dept Quim Analit & Ingn Quim, Madrid 28871, Spain
来源
BIOSENSORS & BIOELECTRONICS | 2009年 / 25卷 / 04期
关键词
Electrodeposition; Gold nanoparticles; DNA biochip; Multimodular; Electrochemical biosensor; SELF-ASSEMBLED MONOLAYERS; DNA BIOSENSORS; COLLOIDAL GOLD; HYBRIDIZATION; PROTEIN; PROBES; POLYNUCLEOTIDES; ANCHOR; SIZE;
D O I
10.1016/j.bios.2009.08.028
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Here, we describe a proof of concept procedure for the selective immobilization of oligonucleotides functionalized gold nanoparticle probes (affinity modules) on arrayed screen-printed gold electrodes. Current microarrays are using many different ways to address their DNA probes onto the transducer area. For that reason, we have mixed the electrodeposition of metals, which is a very well known process, in addition with the DNA-gold nanoparticles formation, which is an area of great interest in biosensing applications in the field of genomics, clinical and warfare applications. Combining these fields, we have developed a novel method for the immobilization of gold nanoparticles conjugated with oligonucleotides (affinity modules) onto screenprinting gold electrodes through electrodeposition at a current positive potential of 800 mV vs. Ag/AgCl. The modules were selectively immobilized onto the electrode surface being, afterwards, ready for a successful hybridization. The gold colloids take the advantage of being a carrier that allows the immobilization of any kind of bioreceptor in the same conditions and the capability of quality control analysis before the electrodeposition procedure. With this system, we avoided non-specific interactions between the transduction layer and the bioreceptor and in the case of DNA oligonucleotides allowed us the immobilization of multiple sequences in a multimodular device for a further industrial process of cheaper biochip fabrication. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:778 / 783
页数:6
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