Fedurco Milan, Romieu Anthony, Williams Scott, Lawrence Isabelle, Turcatti Gerardo
Manteia Predictive Medicine S.A. Zone Industrielle Coinsins, CH-1267, Switzerland.
Nucleic Acids Res. 2006 Feb 9;34(3):e22. doi: 10.1093/nar/gnj023.
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.
三羧酸试剂苯 -1,3,5 - 三乙酸(BTA)用于将5'-氨基化的DNA引物和模板连接到氨基硅烷化的玻璃表面,以便随后通过原位固相扩增生成DNA集落。我们对用于寡核苷酸化学连接的衍生化表面进行了表征,并评估了与扩增过程相关的特性:表面密度、对热循环的热稳定性、功能化重现性和储存稳定性。最初为载玻片开发的衍生化过程随后被应用于包含集成流体连接的微加工玻璃通道。这种改进显著减少了反应时间、试剂消耗并实现了过程自动化。开发了用于表征附着DNA的创新分析方法,以评估扩增后表面固定的DNA含量。所得结果表明,BTA化学方法与固定的初始单模板DNA分子扩增形成具有约1000万个集落/cm²的最佳表面覆盖率的高密度DNA集落阵列兼容且适用。我们还证明,生成的双链DNA集落可通过限制性酶切原位进行定量处理。使用BTA试剂生成的DNA集落可以前所未有的并行方式用于低成本基因组研究的进一步序列分析。