Mitochondrial Precursor Proteins in the Cytosol as Major Determinants of Cellular Health

HORIZON.1.1HORIZON-ERCID: 101052639
EC Contribution
€23,345
Consortium Size
1 orgs
Summary

Mitochondria are made of 800 to 1500 proteins which represent up to 30% of the cellular mass. Owing to their post-translational mode of import, mitochondrial precursor proteins explore the cytosol before they are imported into mitochondria. These reactions are of utmost importance for cellular functionality since cytosolic precursors pose a major threat of cellular proteostasis and are major drivers in aging and for the pathogenesis of neurodegenerative diseases. Still, the biology of cytosolic precursors is largely elusive.In vitro import assays governed the experimentation platform of the mitochondrial community which enabled exquisite breakthroughs in understanding translocation, but are unsuited to elucidate cytosolic reactions. MitoCyto aims to break out of these experimental walls to elucidate the biology of cytosolic precursors with an interdisciplinary research team that leaves the comfort zone of biochemistry to utilize genetic and cell biology approaches but also develops novel cutting-edge techniques from high throughput approaches, through microfluidics-assisted microscopy to synthetic biology. From this innovative combination, detailed mechanistic insights into three so far largely elusive aspects of cell biology will be possible for the first time: (1) What are the cytosolic interactors of mitochondrial precursor proteins? (2) What are the direct and indirect physiological consequences of cytosolic precursor accumulation? (3) How does the re-routing of mitochondrial proteins to the nucleus control growth and fitness of eukaryotic cells?We are convinced that MitoCyto will break grounds to a comprehensive understanding of how eukaryotic cells maintain a healthy proteome over a lifetime despite fluctuating metabolic conditions. While these goals are conceptually deeply rooted in a comprehensive understanding of basic biological questions, they are of immediate relevance for cancer cell metabolism, neurodegeneration and aging.

Consortium (1)

Project Results (7)

Source: CORDIS, the EU research results database.

Publications (7)
Distinct types of intramitochondrial protein aggregates protect mitochondria against proteotoxic stress
Cell Reports· 2024DOI
Lea Bertgen, Jan-Eric Bökenkamp, Tim Schneckmann, Christian Koch, Markus Räschle, Zuzana Storchová, Johannes M. Herrmann
Protein translocation in mitochondria: Sorting out the Toms, Tims, Pams, Sams and Mia
FEBS Letters· 2024DOI
Johannes M Herrmann, Yury Bykov
The ER-SURF pathway uses ER-mitochondria contact sites for protein targeting to mitochondria
EMBO Reports· 2024DOI
Christian Koch; Svenja Lenhard; Markus Räschle; Cristina Prescianotto-Baschong; Anne Spang; Johannes M Herrmann
Membrane insertases at a glance
Journal of Cell Science· 2023DOI
Büsra Kizmaz, Johannes M. Herrmann
The Orf9b protein of SARS-CoV-2 modulates mitochondrial protein biogenesis
The Journal of Cell Biology· 2023DOI
Svenja Lenhard; Sarah Gerlich; Azkia Khan; Saskia Rödl; Jan-Eric Bökenkamp; Esra Peker; Christine Zarges; Janina Faust; Zuzana Storchova; Markus Räschle; Jan Riemer; Johannes M. Herrmann
The role of the proteasome in mitochondrial protein quality control
IUBMB Life· 2023DOI
Saskia Rödl, Johannes M. Herrmann
Mitochondrial dysfunction rapidly modulates the abundance and thermal stability of cellular proteins
Life Science Alliance· 2022DOI
Carina Groh; Per Haberkant; Frank Stein; Sebastian Filbeck; Stefan Pfeffer; Mikhail M Savitski; Felix Boos; Johannes M Herrmann