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Many-molecule encapsulation by an icosahedral shell
We computationally study how an icosahedral shell assembles around hundreds of molecules. Such a process occurs during the formation of the carboxysome, a bacterial microcompartment that assembles around many copies of the enzymes ribulose 1,5-bisphosphate carboxylase/ oxygenase and carbonic anhydra...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947392/ https://www.ncbi.nlm.nih.gov/pubmed/27166515 http://dx.doi.org/10.7554/eLife.14078 |
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author | Perlmutter, Jason D Mohajerani, Farzaneh Hagan, Michael F |
author_facet | Perlmutter, Jason D Mohajerani, Farzaneh Hagan, Michael F |
author_sort | Perlmutter, Jason D |
collection | PubMed |
description | We computationally study how an icosahedral shell assembles around hundreds of molecules. Such a process occurs during the formation of the carboxysome, a bacterial microcompartment that assembles around many copies of the enzymes ribulose 1,5-bisphosphate carboxylase/ oxygenase and carbonic anhydrase to facilitate carbon fixation in cyanobacteria. Our simulations identify two classes of assembly pathways leading to encapsulation of many-molecule cargoes. In one, shell assembly proceeds concomitantly with cargo condensation. In the other, the cargo first forms a dense globule; then, shell proteins assemble around and bud from the condensed cargo complex. Although the model is simplified, the simulations predict intermediates and closure mechanisms not accessible in experiments, and show how assembly can be tuned between these two pathways by modulating protein interactions. In addition to elucidating assembly pathways and critical control parameters for microcompartment assembly, our results may guide the reengineering of viruses as nanoreactors that self-assemble around their reactants. DOI: http://dx.doi.org/10.7554/eLife.14078.001 |
format | Online Article Text |
id | pubmed-4947392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49473922016-07-18 Many-molecule encapsulation by an icosahedral shell Perlmutter, Jason D Mohajerani, Farzaneh Hagan, Michael F eLife Biophysics and Structural Biology We computationally study how an icosahedral shell assembles around hundreds of molecules. Such a process occurs during the formation of the carboxysome, a bacterial microcompartment that assembles around many copies of the enzymes ribulose 1,5-bisphosphate carboxylase/ oxygenase and carbonic anhydrase to facilitate carbon fixation in cyanobacteria. Our simulations identify two classes of assembly pathways leading to encapsulation of many-molecule cargoes. In one, shell assembly proceeds concomitantly with cargo condensation. In the other, the cargo first forms a dense globule; then, shell proteins assemble around and bud from the condensed cargo complex. Although the model is simplified, the simulations predict intermediates and closure mechanisms not accessible in experiments, and show how assembly can be tuned between these two pathways by modulating protein interactions. In addition to elucidating assembly pathways and critical control parameters for microcompartment assembly, our results may guide the reengineering of viruses as nanoreactors that self-assemble around their reactants. DOI: http://dx.doi.org/10.7554/eLife.14078.001 eLife Sciences Publications, Ltd 2016-05-11 /pmc/articles/PMC4947392/ /pubmed/27166515 http://dx.doi.org/10.7554/eLife.14078 Text en © 2016, Perlmutter et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Perlmutter, Jason D Mohajerani, Farzaneh Hagan, Michael F Many-molecule encapsulation by an icosahedral shell |
title | Many-molecule encapsulation by an icosahedral shell |
title_full | Many-molecule encapsulation by an icosahedral shell |
title_fullStr | Many-molecule encapsulation by an icosahedral shell |
title_full_unstemmed | Many-molecule encapsulation by an icosahedral shell |
title_short | Many-molecule encapsulation by an icosahedral shell |
title_sort | many-molecule encapsulation by an icosahedral shell |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947392/ https://www.ncbi.nlm.nih.gov/pubmed/27166515 http://dx.doi.org/10.7554/eLife.14078 |
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