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Nucleic Acids Research 2006 34(3):e22; doi:10.1093/nar/gnj023
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Published online 9 February 2006

© The Author 2006. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions{at}oxfordjournals.org


Methods Online

BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies

Milan Fedurco, Anthony Romieu, Scott Williams, Isabelle Lawrence and Gerardo Turcatti*

Manteia Predictive Medicine S.A. Zone Industrielle Coinsins, CH-1267, Switzerland

*To whom correspondence should be addressed at EPFL, School of life Sciences, Station 15, AAB013, CH-1015, Lausanne Switzerland. Tel: +4121 693 9666; Fax: +4121 693 9667; Email: gerardo.turcatti{at}epfl.ch

Received October 5, 2005. Revised December 1, 2005. Accepted January 25, 2006.

The tricarboxylate reagent benzene-1,3,5-triacetic acid (BTA) was used to attach 5'-aminated DNA primers and templates on an aminosilanized glass surface for subsequent generation of DNA colonies by in situ solid-phase amplification. We have characterized the derivatized surfaces for the chemical attachment of oligonucleotides and evaluate the properties relevant for the amplification process: surface density, thermal stability towards thermocycling, functionalization reproducibility and storage stability. The derivatization process, first developed for glass slides, was then adapted to microfabricated glass channels containing integrated fluidic connections. This implementation resulted in an important reduction of reaction times, consumption of reagents and process automation. Innovative analytical methods for the characterization of attached DNA were developed for assessing the surface immobilized DNA content after amplification. The results obtained showed that the BTA chemistry is compatible and suitable for forming highly dense arrays of DNA colonies with optimal surface coverage of about 10 million colonies/cm2 from the amplification of initial single-template DNA molecules immobilized. We also demonstrate that the dsDNA colonies generated can be quantitatively processed in situ by restriction enzymes digestion. DNA colonies generated using the BTA reagent can be used for further sequence analysis in an unprecedented parallel fashion for low-cost genomic studies.


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