Abstract

Highlights • Reconstruction of mitochondrial protein import and cofactor metabolism in the model eukaryote Saccharomyces cerevisiae • Quantification of the proton motive force shows the significant energy cost of metabolite transport • Protein import activity depends on growth rate and respiratory activity • Quantification iron-sulfur cluster requirements show growth rate dependence

Highlights

  • Mitochondria are a hallmark of eukaryal cells and essential for their viability

  • SUMMARY Mitochondria are a hallmark of eukaryal cells and play an important role in cellular metabolism

  • There is a vast amount of knowledge available on mitochondrial metabolism and essential mitochondrial functions, such as protein import and iron-sulfur cluster biosynthesis, including multiple studies on the mitochondrial proteome

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Summary

Introduction

Mitochondria are a hallmark of eukaryal cells and essential for their viability. Being the center of oxidative phosphorylation, they are often referred to as the powerhouses of the cell, but mitochondria are central to other parts of cellular metabolism and signaling (Malina et al, 2018). Mitochondrial proteomics studies have identified a large fraction of the mitochondrial proteome (Reinders et al, 2006; Sickmann et al, 2003; Vogtle et al, 2012; Vogtle et al, 2017; Zahedi et al, 2006), elucidating numerous mitochondrial functions beyond energy metabolism. These functions include protein import (Wiedemann and Pfanner, 2017) and synthesis of iron-sulfur (Fe/S) clusters (Lill and Freibert, 2020), both essential for cell viability under all conditions. The only moderately altered expression poses a challenge when it comes to experimentally determining the actual levels of proteins involved in Fe/S cluster generation and protein import required to sustain functional mitochondria

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