TY - JOUR
T1 - Definition of a High-Confidence Mitochondrial Proteome at Quantitative Scale
AU - Morgenstern, Marcel
AU - Stiller, Sebastian B.
AU - Lübbert, Philipp
AU - Peikert, Christian D.
AU - Dannenmaier, Stefan
AU - Drepper, Friedel
AU - Weill, Uri
AU - Höß, Philipp
AU - Feuerstein, Reinhild
AU - Gebert, Michael
AU - Bohnert, Maria
AU - van der Laan, Martin
AU - Schuldiner, Maya
AU - Schütze, Conny
AU - Oeljeklaus, Silke
AU - Pfanner, Nikolaus
AU - Wiedemann, Nils
AU - Warscheid, Bettina
N1 - Publisher Copyright: © 2017 The Author(s)
PY - 2017/6/27
Y1 - 2017/6/27
N2 - 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 east 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.
AB - 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 east 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.
UR - http://www.scopus.com/inward/record.url?scp=85021335908&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2017.06.014
DO - 10.1016/j.celrep.2017.06.014
M3 - مقالة
SN - 2211-1247
VL - 19
SP - 2836
EP - 2852
JO - Cell Reports
JF - Cell Reports
IS - 13
ER -