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Light-activated communication in synthetic tissues

We have previously used three-dimensional (3D) printing to prepare tissue-like materials in which picoliter aqueous compartments are separated by lipid bilayers. These printed droplets are elaborated into synthetic cells by using a tightly regulated in vitro transcription/translation system. A light...

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Detalles Bibliográficos
Autores principales: Booth, Michael J., Schild, Vanessa Restrepo, Graham, Alexander D., Olof, Sam N., Bayley, Hagan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820383/
https://www.ncbi.nlm.nih.gov/pubmed/27051884
http://dx.doi.org/10.1126/sciadv.1600056
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author Booth, Michael J.
Schild, Vanessa Restrepo
Graham, Alexander D.
Olof, Sam N.
Bayley, Hagan
author_facet Booth, Michael J.
Schild, Vanessa Restrepo
Graham, Alexander D.
Olof, Sam N.
Bayley, Hagan
author_sort Booth, Michael J.
collection PubMed
description We have previously used three-dimensional (3D) printing to prepare tissue-like materials in which picoliter aqueous compartments are separated by lipid bilayers. These printed droplets are elaborated into synthetic cells by using a tightly regulated in vitro transcription/translation system. A light-activated DNA promoter has been developed that can be used to turn on the expression of any gene within the synthetic cells. We used light activation to express protein pores in 3D-printed patterns within synthetic tissues. The pores are incorporated into specific bilayer interfaces and thereby mediate rapid, directional electrical communication between subsets of cells. Accordingly, we have developed a functional mimic of neuronal transmission that can be controlled in a precise way.
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spelling pubmed-48203832016-04-05 Light-activated communication in synthetic tissues Booth, Michael J. Schild, Vanessa Restrepo Graham, Alexander D. Olof, Sam N. Bayley, Hagan Sci Adv Research Articles We have previously used three-dimensional (3D) printing to prepare tissue-like materials in which picoliter aqueous compartments are separated by lipid bilayers. These printed droplets are elaborated into synthetic cells by using a tightly regulated in vitro transcription/translation system. A light-activated DNA promoter has been developed that can be used to turn on the expression of any gene within the synthetic cells. We used light activation to express protein pores in 3D-printed patterns within synthetic tissues. The pores are incorporated into specific bilayer interfaces and thereby mediate rapid, directional electrical communication between subsets of cells. Accordingly, we have developed a functional mimic of neuronal transmission that can be controlled in a precise way. American Association for the Advancement of Science 2016-04-01 /pmc/articles/PMC4820383/ /pubmed/27051884 http://dx.doi.org/10.1126/sciadv.1600056 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Booth, Michael J.
Schild, Vanessa Restrepo
Graham, Alexander D.
Olof, Sam N.
Bayley, Hagan
Light-activated communication in synthetic tissues
title Light-activated communication in synthetic tissues
title_full Light-activated communication in synthetic tissues
title_fullStr Light-activated communication in synthetic tissues
title_full_unstemmed Light-activated communication in synthetic tissues
title_short Light-activated communication in synthetic tissues
title_sort light-activated communication in synthetic tissues
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820383/
https://www.ncbi.nlm.nih.gov/pubmed/27051884
http://dx.doi.org/10.1126/sciadv.1600056
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