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Repurposing a microfluidic formulation device for automated DNA construction

Microfluidic applications have expanded greatly over the past decade. For the most part, however, each microfluidics platform is developed with a specific task in mind, rather than as a general-purpose device with a wide-range of functionality. Here, we show how a microfluidic system, originally dev...

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Detalles Bibliográficos
Autores principales: Goyal, Garima, Elsbree, Nick, Fero, Michael, Hillson, Nathan J., Linshiz, Gregory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7657503/
https://www.ncbi.nlm.nih.gov/pubmed/33175889
http://dx.doi.org/10.1371/journal.pone.0242157
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author Goyal, Garima
Elsbree, Nick
Fero, Michael
Hillson, Nathan J.
Linshiz, Gregory
author_facet Goyal, Garima
Elsbree, Nick
Fero, Michael
Hillson, Nathan J.
Linshiz, Gregory
author_sort Goyal, Garima
collection PubMed
description Microfluidic applications have expanded greatly over the past decade. For the most part, however, each microfluidics platform is developed with a specific task in mind, rather than as a general-purpose device with a wide-range of functionality. Here, we show how a microfluidic system, originally developed to investigate protein phase behavior, can be modified and repurposed for another application, namely DNA construction. We added new programable controllers to direct the flow of reagents across the chip. We designed the assembly of a combinatorial Golden Gate DNA library using TeselaGen DESIGN software and used the repurposed microfluidics platform to assemble the designed library from off-chip prepared DNA assembly pieces. Further experiments verified the sequences and function of the on-chip assembled DNA constructs.
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spelling pubmed-76575032020-11-18 Repurposing a microfluidic formulation device for automated DNA construction Goyal, Garima Elsbree, Nick Fero, Michael Hillson, Nathan J. Linshiz, Gregory PLoS One Research Article Microfluidic applications have expanded greatly over the past decade. For the most part, however, each microfluidics platform is developed with a specific task in mind, rather than as a general-purpose device with a wide-range of functionality. Here, we show how a microfluidic system, originally developed to investigate protein phase behavior, can be modified and repurposed for another application, namely DNA construction. We added new programable controllers to direct the flow of reagents across the chip. We designed the assembly of a combinatorial Golden Gate DNA library using TeselaGen DESIGN software and used the repurposed microfluidics platform to assemble the designed library from off-chip prepared DNA assembly pieces. Further experiments verified the sequences and function of the on-chip assembled DNA constructs. Public Library of Science 2020-11-11 /pmc/articles/PMC7657503/ /pubmed/33175889 http://dx.doi.org/10.1371/journal.pone.0242157 Text en © 2020 Goyal et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Goyal, Garima
Elsbree, Nick
Fero, Michael
Hillson, Nathan J.
Linshiz, Gregory
Repurposing a microfluidic formulation device for automated DNA construction
title Repurposing a microfluidic formulation device for automated DNA construction
title_full Repurposing a microfluidic formulation device for automated DNA construction
title_fullStr Repurposing a microfluidic formulation device for automated DNA construction
title_full_unstemmed Repurposing a microfluidic formulation device for automated DNA construction
title_short Repurposing a microfluidic formulation device for automated DNA construction
title_sort repurposing a microfluidic formulation device for automated dna construction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7657503/
https://www.ncbi.nlm.nih.gov/pubmed/33175889
http://dx.doi.org/10.1371/journal.pone.0242157
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