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Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase
The mitochondrion of apicomplexan parasites is critical for parasite survival, although the full complement of proteins that localize to this organelle has not been defined. Here we undertake two independent approaches to elucidate the mitochondrial proteome of the apicomplexan Toxoplasma gondii. We...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156079/ https://www.ncbi.nlm.nih.gov/pubmed/30204084 http://dx.doi.org/10.7554/eLife.38131 |
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author | Seidi, Azadeh Muellner-Wong, Linden S Rajendran, Esther Tjhin, Edwin T Dagley, Laura F Aw, Vincent YT Faou, Pierre Webb, Andrew I Tonkin, Christopher J van Dooren, Giel G |
author_facet | Seidi, Azadeh Muellner-Wong, Linden S Rajendran, Esther Tjhin, Edwin T Dagley, Laura F Aw, Vincent YT Faou, Pierre Webb, Andrew I Tonkin, Christopher J van Dooren, Giel G |
author_sort | Seidi, Azadeh |
collection | PubMed |
description | The mitochondrion of apicomplexan parasites is critical for parasite survival, although the full complement of proteins that localize to this organelle has not been defined. Here we undertake two independent approaches to elucidate the mitochondrial proteome of the apicomplexan Toxoplasma gondii. We identify approximately 400 mitochondrial proteins, many of which lack homologs in the animals that these parasites infect, and most of which are important for parasite growth. We demonstrate that one such protein, termed TgApiCox25, is an important component of the parasite cytochrome c oxidase (COX) complex. We identify numerous other apicomplexan-specific components of COX, and conclude that apicomplexan COX, and apicomplexan mitochondria more generally, differ substantially in their protein composition from the hosts they infect. Our study highlights the diversity that exists in mitochondrial proteomes across the eukaryotic domain of life, and provides a foundation for defining unique aspects of mitochondrial biology in an important phylum of parasites. |
format | Online Article Text |
id | pubmed-6156079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61560792018-09-25 Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase Seidi, Azadeh Muellner-Wong, Linden S Rajendran, Esther Tjhin, Edwin T Dagley, Laura F Aw, Vincent YT Faou, Pierre Webb, Andrew I Tonkin, Christopher J van Dooren, Giel G eLife Microbiology and Infectious Disease The mitochondrion of apicomplexan parasites is critical for parasite survival, although the full complement of proteins that localize to this organelle has not been defined. Here we undertake two independent approaches to elucidate the mitochondrial proteome of the apicomplexan Toxoplasma gondii. We identify approximately 400 mitochondrial proteins, many of which lack homologs in the animals that these parasites infect, and most of which are important for parasite growth. We demonstrate that one such protein, termed TgApiCox25, is an important component of the parasite cytochrome c oxidase (COX) complex. We identify numerous other apicomplexan-specific components of COX, and conclude that apicomplexan COX, and apicomplexan mitochondria more generally, differ substantially in their protein composition from the hosts they infect. Our study highlights the diversity that exists in mitochondrial proteomes across the eukaryotic domain of life, and provides a foundation for defining unique aspects of mitochondrial biology in an important phylum of parasites. eLife Sciences Publications, Ltd 2018-09-11 /pmc/articles/PMC6156079/ /pubmed/30204084 http://dx.doi.org/10.7554/eLife.38131 Text en © 2018, Seidi et al http://creativecommons.org/licenses/by/4.0/ 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 | Microbiology and Infectious Disease Seidi, Azadeh Muellner-Wong, Linden S Rajendran, Esther Tjhin, Edwin T Dagley, Laura F Aw, Vincent YT Faou, Pierre Webb, Andrew I Tonkin, Christopher J van Dooren, Giel G Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
title | Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
title_full | Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
title_fullStr | Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
title_full_unstemmed | Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
title_short | Elucidating the mitochondrial proteome of Toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
title_sort | elucidating the mitochondrial proteome of toxoplasma gondii reveals the presence of a divergent cytochrome c oxidase |
topic | Microbiology and Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156079/ https://www.ncbi.nlm.nih.gov/pubmed/30204084 http://dx.doi.org/10.7554/eLife.38131 |
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