Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species
The role of reactive oxygen species (ROS) in signalling and specific targets is not fully understood. Here the authors perform a global proteomic analysis to delineate the yeast redoxome and show that increased levels of intracellular ROS caused by dysfunctional mitochondria decrease global protein...
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2018-01-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-017-02694-8 |
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doaj-dbae8e44a79e41df9b1f9b615b6f89012021-05-11T09:53:56ZengNature Publishing GroupNature Communications2041-17232018-01-019111710.1038/s41467-017-02694-8Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen speciesUlrike Topf0Ida Suppanz1Lukasz Samluk2Lidia Wrobel3Alexander Böser4Paulina Sakowska5Bettina Knapp6Martyna K. Pietrzyk7Agnieszka Chacinska8Bettina Warscheid9International Institute of Molecular and Cell BiologyFaculty of Biology, Institute of Biology II, Biochemistry–Functional Proteomics, University of FreiburgInternational Institute of Molecular and Cell BiologyInternational Institute of Molecular and Cell BiologyFaculty of Biology, Institute of Biology II, Biochemistry–Functional Proteomics, University of FreiburgInternational Institute of Molecular and Cell BiologyFaculty of Biology, Institute of Biology II, Biochemistry–Functional Proteomics, University of FreiburgInternational Institute of Molecular and Cell BiologyInternational Institute of Molecular and Cell BiologyFaculty of Biology, Institute of Biology II, Biochemistry–Functional Proteomics, University of FreiburgThe role of reactive oxygen species (ROS) in signalling and specific targets is not fully understood. Here the authors perform a global proteomic analysis to delineate the yeast redoxome and show that increased levels of intracellular ROS caused by dysfunctional mitochondria decrease global protein synthesis.https://doi.org/10.1038/s41467-017-02694-8 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ulrike Topf Ida Suppanz Lukasz Samluk Lidia Wrobel Alexander Böser Paulina Sakowska Bettina Knapp Martyna K. Pietrzyk Agnieszka Chacinska Bettina Warscheid |
spellingShingle |
Ulrike Topf Ida Suppanz Lukasz Samluk Lidia Wrobel Alexander Böser Paulina Sakowska Bettina Knapp Martyna K. Pietrzyk Agnieszka Chacinska Bettina Warscheid Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species Nature Communications |
author_facet |
Ulrike Topf Ida Suppanz Lukasz Samluk Lidia Wrobel Alexander Böser Paulina Sakowska Bettina Knapp Martyna K. Pietrzyk Agnieszka Chacinska Bettina Warscheid |
author_sort |
Ulrike Topf |
title |
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species |
title_short |
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species |
title_full |
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species |
title_fullStr |
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species |
title_full_unstemmed |
Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species |
title_sort |
quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2018-01-01 |
description |
The role of reactive oxygen species (ROS) in signalling and specific targets is not fully understood. Here the authors perform a global proteomic analysis to delineate the yeast redoxome and show that increased levels of intracellular ROS caused by dysfunctional mitochondria decrease global protein synthesis. |
url |
https://doi.org/10.1038/s41467-017-02694-8 |
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