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Identification of cryptic subunits from an apicomplexan ATP synthase
The mitochondrial ATP synthase is a macromolecular motor that uses the proton gradient to generate ATP. Proper ATP synthase function requires a stator linking the catalytic and rotary portions of the complex. However, sequence-based searches fail to identify genes encoding stator subunits in apicomp...
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/PMC6133553/ https://www.ncbi.nlm.nih.gov/pubmed/30204085 http://dx.doi.org/10.7554/eLife.38097 |
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author | Huet, Diego Rajendran, Esther van Dooren, Giel G Lourido, Sebastian |
author_facet | Huet, Diego Rajendran, Esther van Dooren, Giel G Lourido, Sebastian |
author_sort | Huet, Diego |
collection | PubMed |
description | The mitochondrial ATP synthase is a macromolecular motor that uses the proton gradient to generate ATP. Proper ATP synthase function requires a stator linking the catalytic and rotary portions of the complex. However, sequence-based searches fail to identify genes encoding stator subunits in apicomplexan parasites like Toxoplasma gondii or the related organisms that cause malaria. Here, we identify 11 previously unknown subunits from the Toxoplasma ATP synthase, which lack homologs outside the phylum. Modeling suggests that two of them, ICAP2 and ICAP18, are distantly related to mammalian stator subunits. Our analysis shows that both proteins form part of the ATP synthase complex. Depletion of ICAP2 leads to aberrant mitochondrial morphology, decreased oxygen consumption, and disassembly of the complex, consistent with its role as an essential component of the Toxoplasma ATP synthase. Our findings highlight divergent features of the central metabolic machinery in apicomplexans, which may reveal new therapeutic opportunities. |
format | Online Article Text |
id | pubmed-6133553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61335532018-09-12 Identification of cryptic subunits from an apicomplexan ATP synthase Huet, Diego Rajendran, Esther van Dooren, Giel G Lourido, Sebastian eLife Cell Biology The mitochondrial ATP synthase is a macromolecular motor that uses the proton gradient to generate ATP. Proper ATP synthase function requires a stator linking the catalytic and rotary portions of the complex. However, sequence-based searches fail to identify genes encoding stator subunits in apicomplexan parasites like Toxoplasma gondii or the related organisms that cause malaria. Here, we identify 11 previously unknown subunits from the Toxoplasma ATP synthase, which lack homologs outside the phylum. Modeling suggests that two of them, ICAP2 and ICAP18, are distantly related to mammalian stator subunits. Our analysis shows that both proteins form part of the ATP synthase complex. Depletion of ICAP2 leads to aberrant mitochondrial morphology, decreased oxygen consumption, and disassembly of the complex, consistent with its role as an essential component of the Toxoplasma ATP synthase. Our findings highlight divergent features of the central metabolic machinery in apicomplexans, which may reveal new therapeutic opportunities. eLife Sciences Publications, Ltd 2018-09-11 /pmc/articles/PMC6133553/ /pubmed/30204085 http://dx.doi.org/10.7554/eLife.38097 Text en © 2018, Huet 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 | Cell Biology Huet, Diego Rajendran, Esther van Dooren, Giel G Lourido, Sebastian Identification of cryptic subunits from an apicomplexan ATP synthase |
title | Identification of cryptic subunits from an apicomplexan ATP synthase |
title_full | Identification of cryptic subunits from an apicomplexan ATP synthase |
title_fullStr | Identification of cryptic subunits from an apicomplexan ATP synthase |
title_full_unstemmed | Identification of cryptic subunits from an apicomplexan ATP synthase |
title_short | Identification of cryptic subunits from an apicomplexan ATP synthase |
title_sort | identification of cryptic subunits from an apicomplexan atp synthase |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133553/ https://www.ncbi.nlm.nih.gov/pubmed/30204085 http://dx.doi.org/10.7554/eLife.38097 |
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