Molecular interactions between DNA and an aminated glass substrate

被引:58
作者
Carré, A [1 ]
Lacarrrière, V [1 ]
Birch, W [1 ]
机构
[1] Corning SA, Fontainebleau Res Ctr, F-77210 Avon, France
关键词
DNA; glass; aminosilane; aminopropyltriethoxysilane; surface charge; point of zero charge; ionic interaction; DNA retention; wettability; contact angle; water; pH;
D O I
10.1016/S0021-9797(02)00147-9
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
With the development of DNA arrays, the immobilization of DNA strands onto solid substrates remains an essential research topic. DNA arrays have potential applications in DNA sequencing, mutation detection, and pathogen identification. DNA bound to solid substrates must still be accessible and retain the ability to hybridize with its complementary strands. One technology to produce these arrays involves linking DNA molecule probes to a silanized substrate in microspot patterns and exposing them to a solution of fluorescently labeled samples of DNA targets. The behavior of both the target and probe DNA and their interactions with each other at the substrate surface, particularly with respect to molecular interactions, are poorly understood at the present time. The objective of this work is to model simply the interface interactions between DNA and glass slides modified with an aminosilane (gamma-aminopropyltriethoxysilane, APTS). In aqueous solutions, DNA behaves as a polyacid over a wide range of pH. A glass substrate treated with APTS is positively or negatively charged, depending on the pH. A model of the surface charge of APTS-treated glass has been developed from results of wetting experiments performed at various pH. It has been demonstrated that the surface charge of APTS-treated glass is well described by a model of constant capacitance of the electrical double layer. A good correlation between experimental data on DNA retention at various pH's and the variation of the surface charge of the APTS-treated glass is obtained. This provides an indication of the role of ionic interactions in the adsorption of DNA molecules onto aminated glass slides. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 18 条
[1]   Determination of the main forces driving DNA oligonucleotide adsorption onto aminated silica wafers [J].
Balladur, V ;
Theretz, A ;
Mandrand, B .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1997, 194 (02) :408-418
[2]   ADSORPTION OF DNA TO MICA, SILYLATED MICE, AND MINERALS - CHARACTERIZATION BY ATOMIC-FORCE MICROSCOPY [J].
BEZANILLA, M ;
MANNE, S ;
LANEY, DE ;
LYUBCHENKO, YL ;
HANSMA, HG .
LANGMUIR, 1995, 11 (02) :655-659
[3]  
BIRCH W, 2001, IN PRESS P INT S SUR
[4]  
Birch W., 2000, P EURADH 2000 5 EUR, P242
[5]  
CANTOR CR, 1980, BIOPHYSICAL CHEM, V1
[6]   STUDY OF ACID-BASE PROPERTIES OF OXIDE, OXIDE GLASS, AND GLASS-CERAMIC SURFACES [J].
CARRE, A ;
ROGER, F ;
VARINOT, C .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1992, 154 (01) :174-183
[7]   Effect of hydrophobicity and electrostatics on adsorption and surface diffusion of DNA oligonucleotides at liquid/solid interfaces [J].
Chan, V ;
McKenzie, SE ;
Surrey, S ;
Fortina, P ;
Graves, DJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1998, 203 (01) :197-207
[8]   SURFACE ISOELECTRIC POINT OF EVAPORATED SILVER FILMS - DETERMINATION BY CONTACT-ANGLE TITRATION [J].
CHAU, LK ;
PORTER, MD .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1991, 145 (01) :283-286
[9]   gamma-APTES modified silica gels: The structure of the surface layer [J].
Golub, AA ;
Zubenko, AI ;
Zhmud, BV .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1996, 179 (02) :482-487
[10]   ACIDITY OF SURFACE HYDROXYL GROUPS [J].
HAIR, ML ;
HERTL, W .
JOURNAL OF PHYSICAL CHEMISTRY, 1970, 74 (01) :91-&