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Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids

The use of magnetic bead-immobilized DNA as movable template for cell-free protein synthesis has been investigated. Magnetic microbeads containing chemically conjugated plasmids were used to direct cell-free protein synthesis, so that protein generation could be readily programmed, reset and reprogr...

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Detalles Bibliográficos
Autores principales: Lee, Ka-Young, Lee, Kyung-Ho, Park, Ji-Woong, Kim, Dong-Myung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314631/
https://www.ncbi.nlm.nih.gov/pubmed/22470570
http://dx.doi.org/10.1371/journal.pone.0034429
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author Lee, Ka-Young
Lee, Kyung-Ho
Park, Ji-Woong
Kim, Dong-Myung
author_facet Lee, Ka-Young
Lee, Kyung-Ho
Park, Ji-Woong
Kim, Dong-Myung
author_sort Lee, Ka-Young
collection PubMed
description The use of magnetic bead-immobilized DNA as movable template for cell-free protein synthesis has been investigated. Magnetic microbeads containing chemically conjugated plasmids were used to direct cell-free protein synthesis, so that protein generation could be readily programmed, reset and reprogrammed. Protein synthesis by using this approach could be ON/OFF-controlled through repeated addition and removal of the microbead-conjugated DNA and employed in sequential expression of different genes in a same reaction mixture. Since the incubation periods of individual template plasmids are freely controllable, relative expression levels of multiple proteins can be tuned to desired levels. We expect that the presented results will find wide application to the flexible design and execution of synthetic pathways in cell-free chassis.
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spelling pubmed-33146312012-04-02 Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids Lee, Ka-Young Lee, Kyung-Ho Park, Ji-Woong Kim, Dong-Myung PLoS One Research Article The use of magnetic bead-immobilized DNA as movable template for cell-free protein synthesis has been investigated. Magnetic microbeads containing chemically conjugated plasmids were used to direct cell-free protein synthesis, so that protein generation could be readily programmed, reset and reprogrammed. Protein synthesis by using this approach could be ON/OFF-controlled through repeated addition and removal of the microbead-conjugated DNA and employed in sequential expression of different genes in a same reaction mixture. Since the incubation periods of individual template plasmids are freely controllable, relative expression levels of multiple proteins can be tuned to desired levels. We expect that the presented results will find wide application to the flexible design and execution of synthetic pathways in cell-free chassis. Public Library of Science 2012-03-28 /pmc/articles/PMC3314631/ /pubmed/22470570 http://dx.doi.org/10.1371/journal.pone.0034429 Text en Lee 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lee, Ka-Young
Lee, Kyung-Ho
Park, Ji-Woong
Kim, Dong-Myung
Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids
title Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids
title_full Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids
title_fullStr Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids
title_full_unstemmed Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids
title_short Flexible Programming of Cell-Free Protein Synthesis Using Magnetic Bead-Immobilized Plasmids
title_sort flexible programming of cell-free protein synthesis using magnetic bead-immobilized plasmids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314631/
https://www.ncbi.nlm.nih.gov/pubmed/22470570
http://dx.doi.org/10.1371/journal.pone.0034429
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