Yeast Genetics and Molecular Biology 2002
University of Wisconsin
Madison, Wisconsin USA
July 30 - August 4, 2002


Name: François, Jean M
Mailing Address: CBGD & Genomic Plateform, INSA/University, 135 Av Rangeuil, Toulouse, 31077, FRANCE
Email Address: fran_jm@insa-tlse.fr
Phone & FAX numbers: (33-5)61 55 9492 & (33-5)61 55 9400
URL: http://site.voila.fr/labojmf/index.html

Abstract #489


Session Title: Global Analysis
Presentation: Poster
Topic: Global Analysis

DENDRICHIPS: a New Chip Design based on a novel chemical functionnalisation, which allows higher sensitivity and reusability of DNA-arrays.
Veronique Leberre-Anton (1), Emmanuelle Trevisiol (2), Adilia Dagkessamanskaia (1), Bernard Meunier (3), Jean François (1)
(1) CBGD & Genomic Plateform, INSA/University, 135 Av Rangeuil, Toulouse, 31077, FRANCE; (2) Laboratoire de Chimie de Coordination, 205 Rte de Narbonne,Toulouse.; (3) Laboratoire de Chimie de Coordination, 205 Rte de Narbonne, Toulouse

One of our Research project at the Genomic Platform in Toulouse is concerning the design of better grafting of the DNA on the glass slides to increase both the ratio signal/noise, to obtain higher reproducibility and to be able to reuse the arrays (at least for research purposes). To this end, we developed a new chemical method (the dendrimer technology), whose a EP patent is being obtained Basically, the principle is to bind successively, and in a covalent way, first the dendrimer on a functionalised slide (dendrislide), then the nucleic acids (PCR or oligonucleotides) on the dendrislide to make the dendrichip. As compared to other homemade or commercially available arrays, the main advantages of our technology are as follows. (1) Increase of the sensitivity (signal ratio/noise) by more than 10-fold. (2) Reduction by 10-50-fold of the amount of targets (PCR and oligos) spotted on the dendrislides to reach a equivalent signal as with other DNA microarrays. (3) Ability of re-using at least 10-fold the same dendrichips without decreasing quality and sensitivity of hybridisation. This gives the possibility to repeat the experiment several times in order to obtain statistically reliable results without significant increase of the cost. We will provide comparative results with experiments carried on with yeastgenome.


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