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A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions
Apicomplexan parasites cause major human disease and food insecurity. They owe their considerable success to highly specialized cell compartments and structures. These adaptations drive their recognition, nondestructive penetration, and elaborate reengineering of the host’s cells to promote their gr...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670262/ https://www.ncbi.nlm.nih.gov/pubmed/33053376 http://dx.doi.org/10.1016/j.chom.2020.09.011 |
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author | Barylyuk, Konstantin Koreny, Ludek Ke, Huiling Butterworth, Simon Crook, Oliver M. Lassadi, Imen Gupta, Vipul Tromer, Eelco Mourier, Tobias Stevens, Tim J. Breckels, Lisa M. Pain, Arnab Lilley, Kathryn S. Waller, Ross F. |
author_facet | Barylyuk, Konstantin Koreny, Ludek Ke, Huiling Butterworth, Simon Crook, Oliver M. Lassadi, Imen Gupta, Vipul Tromer, Eelco Mourier, Tobias Stevens, Tim J. Breckels, Lisa M. Pain, Arnab Lilley, Kathryn S. Waller, Ross F. |
author_sort | Barylyuk, Konstantin |
collection | PubMed |
description | Apicomplexan parasites cause major human disease and food insecurity. They owe their considerable success to highly specialized cell compartments and structures. These adaptations drive their recognition, nondestructive penetration, and elaborate reengineering of the host’s cells to promote their growth, dissemination, and the countering of host defenses. The evolution of unique apicomplexan cellular compartments is concomitant with vast proteomic novelty. Consequently, half of apicomplexan proteins are unique and uncharacterized. Here, we determine the steady-state subcellular location of thousands of proteins simultaneously within the globally prevalent apicomplexan parasite Toxoplasma gondii. This provides unprecedented comprehensive molecular definition of these unicellular eukaryotes and their specialized compartments, and these data reveal the spatial organizations of protein expression and function, adaptation to hosts, and the underlying evolutionary trajectories of these pathogens. |
format | Online Article Text |
id | pubmed-7670262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76702622020-11-24 A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions Barylyuk, Konstantin Koreny, Ludek Ke, Huiling Butterworth, Simon Crook, Oliver M. Lassadi, Imen Gupta, Vipul Tromer, Eelco Mourier, Tobias Stevens, Tim J. Breckels, Lisa M. Pain, Arnab Lilley, Kathryn S. Waller, Ross F. Cell Host Microbe Resource Apicomplexan parasites cause major human disease and food insecurity. They owe their considerable success to highly specialized cell compartments and structures. These adaptations drive their recognition, nondestructive penetration, and elaborate reengineering of the host’s cells to promote their growth, dissemination, and the countering of host defenses. The evolution of unique apicomplexan cellular compartments is concomitant with vast proteomic novelty. Consequently, half of apicomplexan proteins are unique and uncharacterized. Here, we determine the steady-state subcellular location of thousands of proteins simultaneously within the globally prevalent apicomplexan parasite Toxoplasma gondii. This provides unprecedented comprehensive molecular definition of these unicellular eukaryotes and their specialized compartments, and these data reveal the spatial organizations of protein expression and function, adaptation to hosts, and the underlying evolutionary trajectories of these pathogens. Cell Press 2020-11-11 /pmc/articles/PMC7670262/ /pubmed/33053376 http://dx.doi.org/10.1016/j.chom.2020.09.011 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Resource Barylyuk, Konstantin Koreny, Ludek Ke, Huiling Butterworth, Simon Crook, Oliver M. Lassadi, Imen Gupta, Vipul Tromer, Eelco Mourier, Tobias Stevens, Tim J. Breckels, Lisa M. Pain, Arnab Lilley, Kathryn S. Waller, Ross F. A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions |
title | A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions |
title_full | A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions |
title_fullStr | A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions |
title_full_unstemmed | A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions |
title_short | A Comprehensive Subcellular Atlas of the Toxoplasma Proteome via hyperLOPIT Provides Spatial Context for Protein Functions |
title_sort | comprehensive subcellular atlas of the toxoplasma proteome via hyperlopit provides spatial context for protein functions |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670262/ https://www.ncbi.nlm.nih.gov/pubmed/33053376 http://dx.doi.org/10.1016/j.chom.2020.09.011 |
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