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Sealable Femtoliter Chamber Arrays for Cell-free Biology
Cell-free systems provide a flexible platform for probing specific networks of biological reactions isolated from the complex resource sharing (e.g., global gene expression, cell division) encountered within living cells. However, such systems, used in conventional macro-scale bulk reactors, often f...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401254/ https://www.ncbi.nlm.nih.gov/pubmed/25867144 http://dx.doi.org/10.3791/52616 |
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author | Norred, Sarah Elizabeth Caveney, Patrick M. Retterer, Scott T. Boreyko, Jonathan B. Fowlkes, Jason D. Collier, Charles Patrick Simpson, Michael L. |
author_facet | Norred, Sarah Elizabeth Caveney, Patrick M. Retterer, Scott T. Boreyko, Jonathan B. Fowlkes, Jason D. Collier, Charles Patrick Simpson, Michael L. |
author_sort | Norred, Sarah Elizabeth |
collection | PubMed |
description | Cell-free systems provide a flexible platform for probing specific networks of biological reactions isolated from the complex resource sharing (e.g., global gene expression, cell division) encountered within living cells. However, such systems, used in conventional macro-scale bulk reactors, often fail to exhibit the dynamic behaviors and efficiencies characteristic of their living micro-scale counterparts. Understanding the impact of internal cell structure and scale on reaction dynamics is crucial to understanding complex gene networks. Here we report a microfabricated device that confines cell-free reactions in cellular scale volumes while allowing flexible characterization of the enclosed molecular system. This multilayered poly(dimethylsiloxane) (PDMS) device contains femtoliter-scale reaction chambers on an elastomeric membrane which can be actuated (open and closed). When actuated, the chambers confine Cell-Free Protein Synthesis (CFPS) reactions expressing a fluorescent protein, allowing for the visualization of the reaction kinetics over time using time-lapse fluorescent microscopy. Here we demonstrate how this device may be used to measure the noise structure of CFPS reactions in a manner that is directly analogous to those used to characterize cellular systems, thereby enabling the use of noise biology techniques used in cellular systems to characterize CFPS gene circuits and their interactions with the cell-free environment. |
format | Online Article Text |
id | pubmed-4401254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-44012542015-04-24 Sealable Femtoliter Chamber Arrays for Cell-free Biology Norred, Sarah Elizabeth Caveney, Patrick M. Retterer, Scott T. Boreyko, Jonathan B. Fowlkes, Jason D. Collier, Charles Patrick Simpson, Michael L. J Vis Exp Bioengineering Cell-free systems provide a flexible platform for probing specific networks of biological reactions isolated from the complex resource sharing (e.g., global gene expression, cell division) encountered within living cells. However, such systems, used in conventional macro-scale bulk reactors, often fail to exhibit the dynamic behaviors and efficiencies characteristic of their living micro-scale counterparts. Understanding the impact of internal cell structure and scale on reaction dynamics is crucial to understanding complex gene networks. Here we report a microfabricated device that confines cell-free reactions in cellular scale volumes while allowing flexible characterization of the enclosed molecular system. This multilayered poly(dimethylsiloxane) (PDMS) device contains femtoliter-scale reaction chambers on an elastomeric membrane which can be actuated (open and closed). When actuated, the chambers confine Cell-Free Protein Synthesis (CFPS) reactions expressing a fluorescent protein, allowing for the visualization of the reaction kinetics over time using time-lapse fluorescent microscopy. Here we demonstrate how this device may be used to measure the noise structure of CFPS reactions in a manner that is directly analogous to those used to characterize cellular systems, thereby enabling the use of noise biology techniques used in cellular systems to characterize CFPS gene circuits and their interactions with the cell-free environment. MyJove Corporation 2015-03-11 /pmc/articles/PMC4401254/ /pubmed/25867144 http://dx.doi.org/10.3791/52616 Text en Copyright © 2015, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Bioengineering Norred, Sarah Elizabeth Caveney, Patrick M. Retterer, Scott T. Boreyko, Jonathan B. Fowlkes, Jason D. Collier, Charles Patrick Simpson, Michael L. Sealable Femtoliter Chamber Arrays for Cell-free Biology |
title | Sealable Femtoliter Chamber Arrays for Cell-free Biology |
title_full | Sealable Femtoliter Chamber Arrays for Cell-free Biology |
title_fullStr | Sealable Femtoliter Chamber Arrays for Cell-free Biology |
title_full_unstemmed | Sealable Femtoliter Chamber Arrays for Cell-free Biology |
title_short | Sealable Femtoliter Chamber Arrays for Cell-free Biology |
title_sort | sealable femtoliter chamber arrays for cell-free biology |
topic | Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401254/ https://www.ncbi.nlm.nih.gov/pubmed/25867144 http://dx.doi.org/10.3791/52616 |
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