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A microfluidic oligonucleotide synthesizer
De novo gene and genome synthesis enables the design of any sequence without the requirement of a pre-existing template as in traditional genetic engineering methods. The ability to mass produce synthetic genes holds great potential for biological research, but widespread availability of de novo DNA...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860119/ https://www.ncbi.nlm.nih.gov/pubmed/20176572 http://dx.doi.org/10.1093/nar/gkq092 |
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author | Lee, Cheng-Chung Snyder, Thomas M. Quake, Stephen R. |
author_facet | Lee, Cheng-Chung Snyder, Thomas M. Quake, Stephen R. |
author_sort | Lee, Cheng-Chung |
collection | PubMed |
description | De novo gene and genome synthesis enables the design of any sequence without the requirement of a pre-existing template as in traditional genetic engineering methods. The ability to mass produce synthetic genes holds great potential for biological research, but widespread availability of de novo DNA constructs is currently hampered by their high cost. In this work, we describe a microfluidic platform for parallel solid phase synthesis of oligonucleotides that can greatly reduce the cost of gene synthesis by reducing reagent consumption (by 100-fold) while maintaining a ∼100 pmol synthesis scale so there is no need for amplification before assembly. Sixteen oligonucleotides were synthesized in parallel on this platform and then successfully used in a ligation-mediated assembly method to generate DNA constructs ∼200 bp in length. |
format | Text |
id | pubmed-2860119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28601192010-04-27 A microfluidic oligonucleotide synthesizer Lee, Cheng-Chung Snyder, Thomas M. Quake, Stephen R. Nucleic Acids Res Synthetic Biology and Chemistry De novo gene and genome synthesis enables the design of any sequence without the requirement of a pre-existing template as in traditional genetic engineering methods. The ability to mass produce synthetic genes holds great potential for biological research, but widespread availability of de novo DNA constructs is currently hampered by their high cost. In this work, we describe a microfluidic platform for parallel solid phase synthesis of oligonucleotides that can greatly reduce the cost of gene synthesis by reducing reagent consumption (by 100-fold) while maintaining a ∼100 pmol synthesis scale so there is no need for amplification before assembly. Sixteen oligonucleotides were synthesized in parallel on this platform and then successfully used in a ligation-mediated assembly method to generate DNA constructs ∼200 bp in length. Oxford University Press 2010-05 2010-02-21 /pmc/articles/PMC2860119/ /pubmed/20176572 http://dx.doi.org/10.1093/nar/gkq092 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 Lee, Cheng-Chung Snyder, Thomas M. Quake, Stephen R. A microfluidic oligonucleotide synthesizer |
title | A microfluidic oligonucleotide synthesizer |
title_full | A microfluidic oligonucleotide synthesizer |
title_fullStr | A microfluidic oligonucleotide synthesizer |
title_full_unstemmed | A microfluidic oligonucleotide synthesizer |
title_short | A microfluidic oligonucleotide synthesizer |
title_sort | microfluidic oligonucleotide synthesizer |
topic | Synthetic Biology and Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860119/ https://www.ncbi.nlm.nih.gov/pubmed/20176572 http://dx.doi.org/10.1093/nar/gkq092 |
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