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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...

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Autores principales: Groh, Carina, Haberkant, Per, Stein, Frank, Filbeck, Sebastian, Pfeffer, Stefan, Savitski, Mikhail M, Boos, Felix, Herrmann, Johannes M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2023
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.
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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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