Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Perlmutter, Jason D, Mohajerani, Farzaneh, Hagan, Michael F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
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
_version_ 1782443169517928448
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
work_keys_str_mv AT perlmutterjasond manymoleculeencapsulationbyanicosahedralshell
AT mohajeranifarzaneh manymoleculeencapsulationbyanicosahedralshell
AT haganmichaelf manymoleculeencapsulationbyanicosahedralshell