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BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies
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 at...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1363783/ https://www.ncbi.nlm.nih.gov/pubmed/16473845 http://dx.doi.org/10.1093/nar/gnj023 |
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author | Fedurco, Milan Romieu, Anthony Williams, Scott Lawrence, Isabelle Turcatti, Gerardo |
author_facet | Fedurco, Milan Romieu, Anthony Williams, Scott Lawrence, Isabelle Turcatti, Gerardo |
author_sort | Fedurco, Milan |
collection | PubMed |
description | 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/cm(2) 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. |
format | Text |
id | pubmed-1363783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-13637832006-02-14 BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies Fedurco, Milan Romieu, Anthony Williams, Scott Lawrence, Isabelle Turcatti, Gerardo Nucleic Acids Res Methods Online 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/cm(2) 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. Oxford University Press 2006 2006-02-09 /pmc/articles/PMC1363783/ /pubmed/16473845 http://dx.doi.org/10.1093/nar/gnj023 Text en © The Author 2006. Published by Oxford University Press. All rights reserved |
spellingShingle | Methods Online Fedurco, Milan Romieu, Anthony Williams, Scott Lawrence, Isabelle Turcatti, Gerardo BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies |
title | BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies |
title_full | BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies |
title_fullStr | BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies |
title_full_unstemmed | BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies |
title_short | BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies |
title_sort | bta, a novel reagent for dna attachment on glass and efficient generation of solid-phase amplified dna colonies |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1363783/ https://www.ncbi.nlm.nih.gov/pubmed/16473845 http://dx.doi.org/10.1093/nar/gnj023 |
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