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Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process
We have achieved the ability to synthesize thousands of unique, long oligonucleotides (150mers) in fmol amounts using parallel synthesis of DNA on microarrays. The sequence accuracy of the oligonucleotides in such large-scale syntheses has been limited by the yields and side reactions of the DNA syn...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860131/ https://www.ncbi.nlm.nih.gov/pubmed/20308161 http://dx.doi.org/10.1093/nar/gkq163 |
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author | LeProust, Emily M. Peck, Bill J. Spirin, Konstantin McCuen, Heather Brummel Moore, Bridget Namsaraev, Eugeni Caruthers, Marvin H. |
author_facet | LeProust, Emily M. Peck, Bill J. Spirin, Konstantin McCuen, Heather Brummel Moore, Bridget Namsaraev, Eugeni Caruthers, Marvin H. |
author_sort | LeProust, Emily M. |
collection | PubMed |
description | We have achieved the ability to synthesize thousands of unique, long oligonucleotides (150mers) in fmol amounts using parallel synthesis of DNA on microarrays. The sequence accuracy of the oligonucleotides in such large-scale syntheses has been limited by the yields and side reactions of the DNA synthesis process used. While there has been significant demand for libraries of long oligos (150mer and more), the yields in conventional DNA synthesis and the associated side reactions have previously limited the availability of oligonucleotide pools to lengths <100 nt. Using novel array based depurination assays, we show that the depurination side reaction is the limiting factor for the synthesis of libraries of long oligonucleotides on Agilent Technologies’ SurePrint® DNA microarray platform. We also demonstrate how depurination can be controlled and reduced by a novel detritylation process to enable the synthesis of high quality, long (150mer) oligonucleotide libraries and we report the characterization of synthesis efficiency for such libraries. Oligonucleotide libraries prepared with this method have changed the economics and availability of several existing applications (e.g. targeted resequencing, preparation of shRNA libraries, site-directed mutagenesis), and have the potential to enable even more novel applications (e.g. high-complexity synthetic biology). |
format | Text |
id | pubmed-2860131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28601312010-04-27 Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process LeProust, Emily M. Peck, Bill J. Spirin, Konstantin McCuen, Heather Brummel Moore, Bridget Namsaraev, Eugeni Caruthers, Marvin H. Nucleic Acids Res Synthetic Biology and Chemistry We have achieved the ability to synthesize thousands of unique, long oligonucleotides (150mers) in fmol amounts using parallel synthesis of DNA on microarrays. The sequence accuracy of the oligonucleotides in such large-scale syntheses has been limited by the yields and side reactions of the DNA synthesis process used. While there has been significant demand for libraries of long oligos (150mer and more), the yields in conventional DNA synthesis and the associated side reactions have previously limited the availability of oligonucleotide pools to lengths <100 nt. Using novel array based depurination assays, we show that the depurination side reaction is the limiting factor for the synthesis of libraries of long oligonucleotides on Agilent Technologies’ SurePrint® DNA microarray platform. We also demonstrate how depurination can be controlled and reduced by a novel detritylation process to enable the synthesis of high quality, long (150mer) oligonucleotide libraries and we report the characterization of synthesis efficiency for such libraries. Oligonucleotide libraries prepared with this method have changed the economics and availability of several existing applications (e.g. targeted resequencing, preparation of shRNA libraries, site-directed mutagenesis), and have the potential to enable even more novel applications (e.g. high-complexity synthetic biology). Oxford University Press 2010-05 2010-03-22 /pmc/articles/PMC2860131/ /pubmed/20308161 http://dx.doi.org/10.1093/nar/gkq163 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Chemistry LeProust, Emily M. Peck, Bill J. Spirin, Konstantin McCuen, Heather Brummel Moore, Bridget Namsaraev, Eugeni Caruthers, Marvin H. Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
title | Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
title_full | Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
title_fullStr | Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
title_full_unstemmed | Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
title_short | Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
title_sort | synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process |
topic | Synthetic Biology and Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860131/ https://www.ncbi.nlm.nih.gov/pubmed/20308161 http://dx.doi.org/10.1093/nar/gkq163 |
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