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Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins
Cellular functionality relies on a well-balanced, but highly dynamic proteome. Dysfunction of mitochondrial protein import leads to the cytosolic accumulation of mitochondrial precursor proteins which compromise cellular proteostasis and trigger a mitoprotein-induced stress response. To dissect the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027898/ https://www.ncbi.nlm.nih.gov/pubmed/36941057 http://dx.doi.org/10.26508/lsa.202201805 |
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author | Groh, Carina Haberkant, Per Stein, Frank Filbeck, Sebastian Pfeffer, Stefan Savitski, Mikhail M Boos, Felix Herrmann, Johannes M |
author_facet | Groh, Carina Haberkant, Per Stein, Frank Filbeck, Sebastian Pfeffer, Stefan Savitski, Mikhail M Boos, Felix Herrmann, Johannes M |
author_sort | Groh, Carina |
collection | PubMed |
description | Cellular functionality relies on a well-balanced, but highly dynamic proteome. Dysfunction of mitochondrial protein import leads to the cytosolic accumulation of mitochondrial precursor proteins which compromise cellular proteostasis and trigger a mitoprotein-induced stress response. To dissect the effects of mitochondrial dysfunction on the cellular proteome as a whole, we developed pre-post thermal proteome profiling. This multiplexed time-resolved proteome-wide thermal stability profiling approach with isobaric peptide tags in combination with a pulsed SILAC labelling elucidated dynamic proteostasis changes in several dimensions: In addition to adaptations in protein abundance, we observed rapid modulations of the thermal stability of individual cellular proteins. Different functional groups of proteins showed characteristic response patterns and reacted with group-specific kinetics, allowing the identification of functional modules that are relevant for mitoprotein-induced stress. Thus, our new pre-post thermal proteome profiling approach uncovered a complex response network that orchestrates proteome homeostasis in eukaryotic cells by time-controlled adaptations of the abundance and the conformation of proteins. |
format | Online Article Text |
id | pubmed-10027898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-100278982023-03-22 Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins Groh, Carina Haberkant, Per Stein, Frank Filbeck, Sebastian Pfeffer, Stefan Savitski, Mikhail M Boos, Felix Herrmann, Johannes M Life Sci Alliance Research Articles Cellular functionality relies on a well-balanced, but highly dynamic proteome. Dysfunction of mitochondrial protein import leads to the cytosolic accumulation of mitochondrial precursor proteins which compromise cellular proteostasis and trigger a mitoprotein-induced stress response. To dissect the effects of mitochondrial dysfunction on the cellular proteome as a whole, we developed pre-post thermal proteome profiling. This multiplexed time-resolved proteome-wide thermal stability profiling approach with isobaric peptide tags in combination with a pulsed SILAC labelling elucidated dynamic proteostasis changes in several dimensions: In addition to adaptations in protein abundance, we observed rapid modulations of the thermal stability of individual cellular proteins. Different functional groups of proteins showed characteristic response patterns and reacted with group-specific kinetics, allowing the identification of functional modules that are relevant for mitoprotein-induced stress. Thus, our new pre-post thermal proteome profiling approach uncovered a complex response network that orchestrates proteome homeostasis in eukaryotic cells by time-controlled adaptations of the abundance and the conformation of proteins. Life Science Alliance LLC 2023-03-20 /pmc/articles/PMC10027898/ /pubmed/36941057 http://dx.doi.org/10.26508/lsa.202201805 Text en © 2023 Groh et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Groh, Carina Haberkant, Per Stein, Frank Filbeck, Sebastian Pfeffer, Stefan Savitski, Mikhail M Boos, Felix Herrmann, Johannes M Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
title | Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
title_full | Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
title_fullStr | Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
title_full_unstemmed | Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
title_short | Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
title_sort | mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027898/ https://www.ncbi.nlm.nih.gov/pubmed/36941057 http://dx.doi.org/10.26508/lsa.202201805 |
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