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Design of Sealable Custom-Shaped Cell Mimicries Based on Self-Assembled Monolayers on CYTOP Polymer
[Image: see text] In bottom-up synthetic biology, one of the major methodological challenges is to provide reaction spaces that mimic biological systems with regard to topology and surface functionality. Of particular interest are cell- or organelle-shaped membrane compartments, as many protein func...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6750829/ https://www.ncbi.nlm.nih.gov/pubmed/31136146 http://dx.doi.org/10.1021/acsami.9b05073 |
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author | Eto, Hiromune Soga, Naoki Franquelim, Henri G. Glock, Philipp Khmelinskaia, Alena Kai, Lei Heymann, Michael Noji, Hiroyuki Schwille, Petra |
author_facet | Eto, Hiromune Soga, Naoki Franquelim, Henri G. Glock, Philipp Khmelinskaia, Alena Kai, Lei Heymann, Michael Noji, Hiroyuki Schwille, Petra |
author_sort | Eto, Hiromune |
collection | PubMed |
description | [Image: see text] In bottom-up synthetic biology, one of the major methodological challenges is to provide reaction spaces that mimic biological systems with regard to topology and surface functionality. Of particular interest are cell- or organelle-shaped membrane compartments, as many protein functions unfold at lipid interfaces. However, shaping artificial cell systems using materials with non-intrusive physicochemical properties, while maintaining flexible lipid interfaces relevant to the reconstituted protein systems, is not straightforward. Herein, we develop micropatterned chambers from CYTOP, a less commonly used polymer with good chemical resistance and a refractive index matching that of water. By forming a self-assembled lipid monolayer on the polymer surface, we dramatically increased the biocompatibility of CYTOP-fabricated systems. The phospholipid interface provides an excellent passivation layer to prevent protein adhesion to the hydrophobic surface, and we succeeded in cell-free protein synthesis inside the chambers. Importantly, the chambers could be sealed after loading by a lipid monolayer, providing a novel platform to study encapsulated systems. We successfully reconstituted pole-to-pole oscillations of the Escherichia coli MinDE system, which responds dramatically to compartment geometry. Furthermore, we present a simplified fabrication of our artificial cell compartments via replica molding, making it a readily accessible technique for standard cleanroom facilities. |
format | Online Article Text |
id | pubmed-6750829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-67508292019-09-19 Design of Sealable Custom-Shaped Cell Mimicries Based on Self-Assembled Monolayers on CYTOP Polymer Eto, Hiromune Soga, Naoki Franquelim, Henri G. Glock, Philipp Khmelinskaia, Alena Kai, Lei Heymann, Michael Noji, Hiroyuki Schwille, Petra ACS Appl Mater Interfaces [Image: see text] In bottom-up synthetic biology, one of the major methodological challenges is to provide reaction spaces that mimic biological systems with regard to topology and surface functionality. Of particular interest are cell- or organelle-shaped membrane compartments, as many protein functions unfold at lipid interfaces. However, shaping artificial cell systems using materials with non-intrusive physicochemical properties, while maintaining flexible lipid interfaces relevant to the reconstituted protein systems, is not straightforward. Herein, we develop micropatterned chambers from CYTOP, a less commonly used polymer with good chemical resistance and a refractive index matching that of water. By forming a self-assembled lipid monolayer on the polymer surface, we dramatically increased the biocompatibility of CYTOP-fabricated systems. The phospholipid interface provides an excellent passivation layer to prevent protein adhesion to the hydrophobic surface, and we succeeded in cell-free protein synthesis inside the chambers. Importantly, the chambers could be sealed after loading by a lipid monolayer, providing a novel platform to study encapsulated systems. We successfully reconstituted pole-to-pole oscillations of the Escherichia coli MinDE system, which responds dramatically to compartment geometry. Furthermore, we present a simplified fabrication of our artificial cell compartments via replica molding, making it a readily accessible technique for standard cleanroom facilities. American Chemical Society 2019-05-28 2019-06-19 /pmc/articles/PMC6750829/ /pubmed/31136146 http://dx.doi.org/10.1021/acsami.9b05073 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Eto, Hiromune Soga, Naoki Franquelim, Henri G. Glock, Philipp Khmelinskaia, Alena Kai, Lei Heymann, Michael Noji, Hiroyuki Schwille, Petra Design of Sealable Custom-Shaped Cell Mimicries Based on Self-Assembled Monolayers on CYTOP Polymer |
title | Design
of Sealable Custom-Shaped Cell Mimicries Based
on Self-Assembled Monolayers on CYTOP Polymer |
title_full | Design
of Sealable Custom-Shaped Cell Mimicries Based
on Self-Assembled Monolayers on CYTOP Polymer |
title_fullStr | Design
of Sealable Custom-Shaped Cell Mimicries Based
on Self-Assembled Monolayers on CYTOP Polymer |
title_full_unstemmed | Design
of Sealable Custom-Shaped Cell Mimicries Based
on Self-Assembled Monolayers on CYTOP Polymer |
title_short | Design
of Sealable Custom-Shaped Cell Mimicries Based
on Self-Assembled Monolayers on CYTOP Polymer |
title_sort | design
of sealable custom-shaped cell mimicries based
on self-assembled monolayers on cytop polymer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6750829/ https://www.ncbi.nlm.nih.gov/pubmed/31136146 http://dx.doi.org/10.1021/acsami.9b05073 |
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