Innovative metal oxide-based substrates for DNA microarrays

被引:13
作者
Armelao, Lidia [1 ,2 ]
Pascolini, Michele [1 ,2 ]
Biasiolo, Elena
Tondello, Eugenio [1 ]
Bottaro, Gregorio [3 ,4 ]
Carbonare, Maurizio Dalle [5 ]
D'Arrigo, Antonello [5 ]
Leon, Alberta [5 ]
机构
[1] Univ Padua, Dipartimento Sci Chim, ISTM, CNR, I-35131 Padua, Italy
[2] Univ Padua, Dipartimento Sci Chim, INSTM, I-35131 Padua, Italy
[3] CNR, IMIP, I-70126 Bari, Italy
[4] INSTM, I-70126 Bari, Italy
[5] Res & Innovat Co, I-35127 Padua, Italy
关键词
sol-gel; DNA microarrays; iron oxide; zinc oxide; functional surfaces;
D O I
10.1016/j.ica.2008.03.121
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In the present report, we propose a novel approach to synthesize DNA microarrays that employs immobilization of the nucleic acid molecules onto zinc and iron oxide surfaces through their phosphate backbone. Oxide films were prepared by the sol-gel technique and the resulting surfaces were characterized especially with respect to surface chemistry and morphological features by both X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). ZnO films annealed at T <= 300 degrees C show the most promising surface features to be employed for DNA microarray preparation, i.e. high density of binding sites (hydroxyl groups), smooth and homogeneous surfaces, high optical transmittance in the visible spectral range suitable for detection using fluorescence, and easy handling during preparation procedures. The analysis of nucleic acid retention on the oxide layers was performed by the scanning of dye-labelled DNA previously printed on the substrate using the DNA microarray robotic arm. Clearly visible spots with regular shape were revealed above the background noise indicating that anchoring of the DNA on the treated surface is efficient and does not interfere with hybridization processes. The use of suitably engineered zinc oxide film makes the immobilization strategy ideal for facile, efficient, and cost-effective manufacturing of DNA microarrays. (c) 2008 Published by Elsevier B.V.
引用
收藏
页码:3603 / 3608
页数:6
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