Dendrimeric coating of glass slides for sensitive DNA microarrays analysis -: art. no. e88

被引:132
作者
Le Berre, V
Trévisiol, E
Dagkessamanskaia, A
Sokol, S
Caminade, AM
Majoral, JP
Meunier, B
François, J [1 ]
机构
[1] Inst Natl Sci Appl, Transcriptome Biochips Platform Genopole Toulouse, F-31077 Toulouse 04, France
[2] Inst Natl Sci Appl, Ctr Bioingn Gilbert Durand, CNRS, UMR 5504,UMR INRA 792, F-31077 Toulouse, France
[3] CNRS, Chim Coordinat Lab, F-31077 Toulouse 04, France
关键词
D O I
10.1093/nar/gng088
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Successful use and reliability of microarray technology is highly dependent on several factors, including surface chemistry parameters and accessibility of cDNA targets to the DNA probes fixed onto the surface. Here, we show that functionalisation of glass slides with homemade dendrimers allow production of more sensitive and reliable DNA microarrays. The dendrimers are nanometric structures of size-controlled diameter with aldehyde function at their periphery. Covalent attachment of these spherical reactive chemical structures on amino-silanised glass slides generates a reactive similar to100 Angstrom layer onto which amino-modified DNA probes are covalently bound. This new grafting chemistry leads to the formation of uniform and homogenous spots. More over, probe concentration before spotting could be reduced from 0.2 to 0.02 mg/ml with PCR products and from 20 to 5 muM with 70mer oligonucleotides without affecting signal intensities after hybridisation with Cy3- and Cy5-labelled targets. More interestingly, while the binding capacity of captured probes on dendrimer-activated glass surface (named dendrislides) is roughly similar to other functionalised glass slides from commercial sources, detection sensitivity was 2-fold higher than with other available DNA microarrays. This detection limit was estimated to 0.1 pM of cDNA targets. Altogether, these features make dendrimer-activated slides ideal for manufacturing cost-effective DNA arrays applicable for gene expression and detection of mutations.
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页数:8
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