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A scalable method for multiplex LED-controlled synthesis of DNA in capillaries

As research in synthetic biology and genomic sciences becomes more widespread, the need for diverse oligonucleotide populations has increased. To limit reagent cost, it would be advantageous to obtain high quality populations in minute amounts. Towards that end, synthesis of DNA strands in capillari...

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Detalles Bibliográficos
Autores principales: Blair, Sarah, Richmond, Kathryn, Rodesch, Matthew, Bassetti, Michael, Cerrina, Franco
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636377/
https://www.ncbi.nlm.nih.gov/pubmed/16963493
http://dx.doi.org/10.1093/nar/gkl641
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author Blair, Sarah
Richmond, Kathryn
Rodesch, Matthew
Bassetti, Michael
Cerrina, Franco
author_facet Blair, Sarah
Richmond, Kathryn
Rodesch, Matthew
Bassetti, Michael
Cerrina, Franco
author_sort Blair, Sarah
collection PubMed
description As research in synthetic biology and genomic sciences becomes more widespread, the need for diverse oligonucleotide populations has increased. To limit reagent cost, it would be advantageous to obtain high quality populations in minute amounts. Towards that end, synthesis of DNA strands in capillaries utilizing photolabile 3-nitrophenylpropyloxycarbonyl (NPPOC) chemistry and ultraviolet-light emitting diodes (UV-LEDs) was examined. Multiple oligonucleotides were made in single capillaries and were characterized by hybridization, sequencing and gene synthesis. DNA synthesized in capillaries was capable of being hybridized and signal intensities correlated with microarray data. Sequencing demonstrated that the oligonucleotides were of high quality (up to 44% perfect sequences). Oligonucleotides were combined and used successfully for gene synthesis. This system offers a novel, scalable method to synthesize high quality oligonucleotides for biological applications.
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spelling pubmed-16363772006-11-29 A scalable method for multiplex LED-controlled synthesis of DNA in capillaries Blair, Sarah Richmond, Kathryn Rodesch, Matthew Bassetti, Michael Cerrina, Franco Nucleic Acids Res Methods Online As research in synthetic biology and genomic sciences becomes more widespread, the need for diverse oligonucleotide populations has increased. To limit reagent cost, it would be advantageous to obtain high quality populations in minute amounts. Towards that end, synthesis of DNA strands in capillaries utilizing photolabile 3-nitrophenylpropyloxycarbonyl (NPPOC) chemistry and ultraviolet-light emitting diodes (UV-LEDs) was examined. Multiple oligonucleotides were made in single capillaries and were characterized by hybridization, sequencing and gene synthesis. DNA synthesized in capillaries was capable of being hybridized and signal intensities correlated with microarray data. Sequencing demonstrated that the oligonucleotides were of high quality (up to 44% perfect sequences). Oligonucleotides were combined and used successfully for gene synthesis. This system offers a novel, scalable method to synthesize high quality oligonucleotides for biological applications. Oxford University Press 2006-09 2006-09-08 /pmc/articles/PMC1636377/ /pubmed/16963493 http://dx.doi.org/10.1093/nar/gkl641 Text en © 2006 The Author(s)
spellingShingle Methods Online
Blair, Sarah
Richmond, Kathryn
Rodesch, Matthew
Bassetti, Michael
Cerrina, Franco
A scalable method for multiplex LED-controlled synthesis of DNA in capillaries
title A scalable method for multiplex LED-controlled synthesis of DNA in capillaries
title_full A scalable method for multiplex LED-controlled synthesis of DNA in capillaries
title_fullStr A scalable method for multiplex LED-controlled synthesis of DNA in capillaries
title_full_unstemmed A scalable method for multiplex LED-controlled synthesis of DNA in capillaries
title_short A scalable method for multiplex LED-controlled synthesis of DNA in capillaries
title_sort scalable method for multiplex led-controlled synthesis of dna in capillaries
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636377/
https://www.ncbi.nlm.nih.gov/pubmed/16963493
http://dx.doi.org/10.1093/nar/gkl641
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