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Sustained enzymatic activity and flow in crowded protein droplets

Living cells harvest energy from their environments to drive the chemical processes that enable life. We introduce a minimal system that operates at similar protein concentrations, metabolic densities, and length scales as living cells. This approach takes advantage of the tendency of phase-separate...

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Autores principales: Testa, Andrea, Dindo, Mirco, Rebane, Aleksander A., Nasouri, Babak, Style, Robert W., Golestanian, Ramin, Dufresne, Eric R., Laurino, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560906/
https://www.ncbi.nlm.nih.gov/pubmed/34725341
http://dx.doi.org/10.1038/s41467-021-26532-0
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author Testa, Andrea
Dindo, Mirco
Rebane, Aleksander A.
Nasouri, Babak
Style, Robert W.
Golestanian, Ramin
Dufresne, Eric R.
Laurino, Paola
author_facet Testa, Andrea
Dindo, Mirco
Rebane, Aleksander A.
Nasouri, Babak
Style, Robert W.
Golestanian, Ramin
Dufresne, Eric R.
Laurino, Paola
author_sort Testa, Andrea
collection PubMed
description Living cells harvest energy from their environments to drive the chemical processes that enable life. We introduce a minimal system that operates at similar protein concentrations, metabolic densities, and length scales as living cells. This approach takes advantage of the tendency of phase-separated protein droplets to strongly partition enzymes, while presenting minimal barriers to transport of small molecules across their interface. By dispersing these microreactors in a reservoir of substrate-loaded buffer, we achieve steady states at metabolic densities that match those of the hungriest microorganisms. We further demonstrate the formation of steady pH gradients, capable of driving microscopic flows. Our approach enables the investigation of the function of diverse enzymes in environments that mimic cytoplasm, and provides a flexible platform for studying the collective behavior of matter driven far from equilibrium.
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spelling pubmed-85609062021-11-15 Sustained enzymatic activity and flow in crowded protein droplets Testa, Andrea Dindo, Mirco Rebane, Aleksander A. Nasouri, Babak Style, Robert W. Golestanian, Ramin Dufresne, Eric R. Laurino, Paola Nat Commun Article Living cells harvest energy from their environments to drive the chemical processes that enable life. We introduce a minimal system that operates at similar protein concentrations, metabolic densities, and length scales as living cells. This approach takes advantage of the tendency of phase-separated protein droplets to strongly partition enzymes, while presenting minimal barriers to transport of small molecules across their interface. By dispersing these microreactors in a reservoir of substrate-loaded buffer, we achieve steady states at metabolic densities that match those of the hungriest microorganisms. We further demonstrate the formation of steady pH gradients, capable of driving microscopic flows. Our approach enables the investigation of the function of diverse enzymes in environments that mimic cytoplasm, and provides a flexible platform for studying the collective behavior of matter driven far from equilibrium. Nature Publishing Group UK 2021-11-01 /pmc/articles/PMC8560906/ /pubmed/34725341 http://dx.doi.org/10.1038/s41467-021-26532-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Testa, Andrea
Dindo, Mirco
Rebane, Aleksander A.
Nasouri, Babak
Style, Robert W.
Golestanian, Ramin
Dufresne, Eric R.
Laurino, Paola
Sustained enzymatic activity and flow in crowded protein droplets
title Sustained enzymatic activity and flow in crowded protein droplets
title_full Sustained enzymatic activity and flow in crowded protein droplets
title_fullStr Sustained enzymatic activity and flow in crowded protein droplets
title_full_unstemmed Sustained enzymatic activity and flow in crowded protein droplets
title_short Sustained enzymatic activity and flow in crowded protein droplets
title_sort sustained enzymatic activity and flow in crowded protein droplets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560906/
https://www.ncbi.nlm.nih.gov/pubmed/34725341
http://dx.doi.org/10.1038/s41467-021-26532-0
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