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One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells

[Image: see text] Here, we introduce a one-pot method for the bottom-up assembly of complex single- and multicompartment synthetic cells. Cellular components are enclosed within giant unilamellar vesicles (GUVs), produced at the milliliter scale directly from small unilamellar vesicles (SUVs) or pro...

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Autores principales: Göpfrich, Kerstin, Haller, Barbara, Staufer, Oskar, Dreher, Yannik, Mersdorf, Ulrike, Platzman, Ilia, Spatz, Joachim P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528161/
https://www.ncbi.nlm.nih.gov/pubmed/31042361
http://dx.doi.org/10.1021/acssynbio.9b00034
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author Göpfrich, Kerstin
Haller, Barbara
Staufer, Oskar
Dreher, Yannik
Mersdorf, Ulrike
Platzman, Ilia
Spatz, Joachim P.
author_facet Göpfrich, Kerstin
Haller, Barbara
Staufer, Oskar
Dreher, Yannik
Mersdorf, Ulrike
Platzman, Ilia
Spatz, Joachim P.
author_sort Göpfrich, Kerstin
collection PubMed
description [Image: see text] Here, we introduce a one-pot method for the bottom-up assembly of complex single- and multicompartment synthetic cells. Cellular components are enclosed within giant unilamellar vesicles (GUVs), produced at the milliliter scale directly from small unilamellar vesicles (SUVs) or proteoliposomes with only basic laboratory equipment within minutes. Toward this end, we layer an aqueous solution, containing SUVs and all biocomponents, on top of an oil–surfactant mix. Manual shaking induces the spontaneous formation of surfactant-stabilized water-in-oil droplets with a spherical supported lipid bilayer at their periphery. Finally, to release GUV-based synthetic cells from the oil and the surfactant shell into the physiological environment, we add an aqueous buffer and a droplet-destabilizing agent. We prove that the obtained GUVs are unilamellar by reconstituting the pore-forming membrane protein α-hemolysin and assess the membrane quality with cryotransmission electron microscopy (cryoTEM), fluorescence recovery after photobleaching (FRAP), and zeta-potential measurements as well as confocal fluorescence imaging. We further demonstrate that our GUV formation method overcomes key challenges of standard techniques, offering high volumes, a flexible choice of lipid compositions and buffer conditions, straightforward coreconstitution of proteins, and a high encapsulation efficiency of biomolecules and even large cargo including cells. We thereby provide a simple, robust, and broadly applicable strategy to mass-produce complex multicomponent GUVs for high-throughput testing in synthetic biology and biomedicine, which can directly be implemented in laboratories around the world.
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spelling pubmed-65281612019-05-22 One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells Göpfrich, Kerstin Haller, Barbara Staufer, Oskar Dreher, Yannik Mersdorf, Ulrike Platzman, Ilia Spatz, Joachim P. ACS Synth Biol [Image: see text] Here, we introduce a one-pot method for the bottom-up assembly of complex single- and multicompartment synthetic cells. Cellular components are enclosed within giant unilamellar vesicles (GUVs), produced at the milliliter scale directly from small unilamellar vesicles (SUVs) or proteoliposomes with only basic laboratory equipment within minutes. Toward this end, we layer an aqueous solution, containing SUVs and all biocomponents, on top of an oil–surfactant mix. Manual shaking induces the spontaneous formation of surfactant-stabilized water-in-oil droplets with a spherical supported lipid bilayer at their periphery. Finally, to release GUV-based synthetic cells from the oil and the surfactant shell into the physiological environment, we add an aqueous buffer and a droplet-destabilizing agent. We prove that the obtained GUVs are unilamellar by reconstituting the pore-forming membrane protein α-hemolysin and assess the membrane quality with cryotransmission electron microscopy (cryoTEM), fluorescence recovery after photobleaching (FRAP), and zeta-potential measurements as well as confocal fluorescence imaging. We further demonstrate that our GUV formation method overcomes key challenges of standard techniques, offering high volumes, a flexible choice of lipid compositions and buffer conditions, straightforward coreconstitution of proteins, and a high encapsulation efficiency of biomolecules and even large cargo including cells. We thereby provide a simple, robust, and broadly applicable strategy to mass-produce complex multicomponent GUVs for high-throughput testing in synthetic biology and biomedicine, which can directly be implemented in laboratories around the world. American Chemical Society 2019-05-01 2019-05-17 /pmc/articles/PMC6528161/ /pubmed/31042361 http://dx.doi.org/10.1021/acssynbio.9b00034 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 Göpfrich, Kerstin
Haller, Barbara
Staufer, Oskar
Dreher, Yannik
Mersdorf, Ulrike
Platzman, Ilia
Spatz, Joachim P.
One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
title One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
title_full One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
title_fullStr One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
title_full_unstemmed One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
title_short One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
title_sort one-pot assembly of complex giant unilamellar vesicle-based synthetic cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6528161/
https://www.ncbi.nlm.nih.gov/pubmed/31042361
http://dx.doi.org/10.1021/acssynbio.9b00034
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