Cell Reports
Volume 19, Issue 13, 27 June 2017, Pages 2836-2852
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Definition of a High-Confidence Mitochondrial Proteome at Quantitative Scale

https://doi.org/10.1016/j.celrep.2017.06.014Get rights and content
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Highlights

  • Classification of > 3,300 proteins of mitochondria and associated fractions

  • High-confidence mitochondrial proteome with absolute quantification and topology

  • Interactors of oxidative phosphorylation complexes and cristae organizing system

  • Identification of system linking respiratory chain and AAA quality control

Summary

Mitochondria perform central functions in cellular bioenergetics, metabolism, and signaling, and their dysfunction has been linked to numerous diseases. The available studies cover only part of the mitochondrial proteome, and a separation of core mitochondrial proteins from associated fractions has not been achieved. We developed an integrative experimental approach to define the proteome of yeast mitochondria. We classified > 3,300 proteins of mitochondria and mitochondria-associated fractions and defined 901 high-confidence mitochondrial proteins, expanding the set of mitochondrial proteins by 82. Our analysis includes protein abundance under fermentable and nonfermentable growth, submitochondrial localization, single-protein experiments, and subcellular classification of mitochondria-associated fractions. We identified mitochondrial interactors of respiratory chain supercomplexes, ATP synthase, AAA proteases, the mitochondrial contact site and cristae organizing system (MICOS), and the coenzyme Q biosynthesis cluster, as well as mitochondrial proteins with dual cellular localization. The integrative proteome provides a high-confidence source for the characterization of physiological and pathophysiological functions of mitochondria and their integration into the cellular environment.

Keywords

mitochondria
quantitative MS
protein-protein interaction
subcellular localization
SILAC
protein copy numbers
submitochondrial localization
dual localization

Cited by (0)

7

These authors contributed equally

8

Present address: Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany

9

Present address: Center for Chronic Immunodeficiency, Medical Center, University of Freiburg, 79106 Freiburg, Germany

10

Present address: Baxter Deutschland GmbH, 72379 Hechingen, Germany

11

Present address: Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 7610001, Israel

12

Lead Contact