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Shaping Liposomes by Cell-Free Expressed Bacterial Microtubules
[Image: see text] Genetic control over a cytoskeletal network inside lipid vesicles offers a potential route to controlled shape changes and DNA segregation in synthetic cell biology. Bacterial microtubules (bMTs) are protein filaments found in bacteria of the genus Prosthecobacter. They are formed...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524656/ https://www.ncbi.nlm.nih.gov/pubmed/34585918 http://dx.doi.org/10.1021/acssynbio.1c00278 |
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author | Kattan, Johannes Doerr, Anne Dogterom, Marileen Danelon, Christophe |
author_facet | Kattan, Johannes Doerr, Anne Dogterom, Marileen Danelon, Christophe |
author_sort | Kattan, Johannes |
collection | PubMed |
description | [Image: see text] Genetic control over a cytoskeletal network inside lipid vesicles offers a potential route to controlled shape changes and DNA segregation in synthetic cell biology. Bacterial microtubules (bMTs) are protein filaments found in bacteria of the genus Prosthecobacter. They are formed by the tubulins BtubA and BtubB, which polymerize in the presence of GTP. Here, we show that the tubulins BtubA/B can be functionally expressed from DNA templates in a reconstituted transcription-translation system, thus providing a cytosol-like environment to study their biochemical and biophysical properties. We found that bMTs spontaneously interact with lipid membranes and display treadmilling. When compartmentalized inside liposomes, de novo synthesized BtubA/B tubulins self-organize into cytoskeletal structures of different morphologies. Moreover, bMTs can exert a pushing force on the membrane and deform liposomes, a phenomenon that can be reversed by a light-activated disassembly of the filaments. Our work establishes bMTs as a new building block in synthetic biology. In the context of creating a synthetic cell, bMTs could help shape the lipid compartment, establish polarity or directional transport, and assist the division machinery. |
format | Online Article Text |
id | pubmed-8524656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85246562021-10-20 Shaping Liposomes by Cell-Free Expressed Bacterial Microtubules Kattan, Johannes Doerr, Anne Dogterom, Marileen Danelon, Christophe ACS Synth Biol [Image: see text] Genetic control over a cytoskeletal network inside lipid vesicles offers a potential route to controlled shape changes and DNA segregation in synthetic cell biology. Bacterial microtubules (bMTs) are protein filaments found in bacteria of the genus Prosthecobacter. They are formed by the tubulins BtubA and BtubB, which polymerize in the presence of GTP. Here, we show that the tubulins BtubA/B can be functionally expressed from DNA templates in a reconstituted transcription-translation system, thus providing a cytosol-like environment to study their biochemical and biophysical properties. We found that bMTs spontaneously interact with lipid membranes and display treadmilling. When compartmentalized inside liposomes, de novo synthesized BtubA/B tubulins self-organize into cytoskeletal structures of different morphologies. Moreover, bMTs can exert a pushing force on the membrane and deform liposomes, a phenomenon that can be reversed by a light-activated disassembly of the filaments. Our work establishes bMTs as a new building block in synthetic biology. In the context of creating a synthetic cell, bMTs could help shape the lipid compartment, establish polarity or directional transport, and assist the division machinery. American Chemical Society 2021-09-29 2021-10-15 /pmc/articles/PMC8524656/ /pubmed/34585918 http://dx.doi.org/10.1021/acssynbio.1c00278 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Kattan, Johannes Doerr, Anne Dogterom, Marileen Danelon, Christophe Shaping Liposomes by Cell-Free Expressed Bacterial Microtubules |
title | Shaping Liposomes by Cell-Free Expressed Bacterial
Microtubules |
title_full | Shaping Liposomes by Cell-Free Expressed Bacterial
Microtubules |
title_fullStr | Shaping Liposomes by Cell-Free Expressed Bacterial
Microtubules |
title_full_unstemmed | Shaping Liposomes by Cell-Free Expressed Bacterial
Microtubules |
title_short | Shaping Liposomes by Cell-Free Expressed Bacterial
Microtubules |
title_sort | shaping liposomes by cell-free expressed bacterial
microtubules |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524656/ https://www.ncbi.nlm.nih.gov/pubmed/34585918 http://dx.doi.org/10.1021/acssynbio.1c00278 |
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