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Mic60 exhibits a coordinated clustered distribution along and across yeast and mammalian mitochondria.
Stoldt, Stefan; Stephan, Till; Jans, Daniel C; Brüser, Christian; Lange, Felix; Keller-Findeisen, Jan; Riedel, Dietmar; Hell, Stefan W; Jakobs, Stefan.
Afiliação
  • Stoldt S; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Stephan T; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Jans DC; Clinic of Neurology, University Medical Center Göttingen, 37075 Göttingen, Germany.
  • Brüser C; Science for Life Laboratory, Department of Applied Physics, Royal Institute of Technology, 171 65 Stockholm, Sweden.
  • Lange F; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Keller-Findeisen J; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Riedel D; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Hell SW; Laboratory of Electron Microscopy, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
  • Jakobs S; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany; stefan.hell@mpibpc.mpg.de sjakobs@gwdg.de.
Proc Natl Acad Sci U S A ; 116(20): 9853-9858, 2019 05 14.
Article em En | MEDLINE | ID: mdl-31028145
ABSTRACT
Mitochondria are tubular double-membrane organelles essential for eukaryotic life. They form extended networks and exhibit an intricate inner membrane architecture. The MICOS (mitochondrial contact site and cristae organizing system) complex, crucial for proper architecture of the mitochondrial inner membrane, is localized primarily at crista junctions. Harnessing superresolution fluorescence microscopy, we demonstrate that Mic60, a subunit of the MICOS complex, as well as several of its interaction partners are arranged into intricate patterns in human and yeast mitochondria, suggesting an ordered distribution of the crista junctions. We show that Mic60 forms clusters that are preferentially localized in the inner membrane at two opposing sides of the mitochondrial tubules so that they form extended opposing distribution bands. These Mic60 distribution bands can be twisted, resulting in a helical arrangement. Focused ion beam milling-scanning electron microscopy showed that in yeast the twisting of the opposing distribution bands is echoed by the folding of the inner membrane. We show that establishment of the Mic60 distribution bands is largely independent of the cristae morphology. We suggest that Mic60 is part of an extended multiprotein interaction network that scaffolds mitochondria.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Mitocondriais / Membranas Mitocondriais Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Mitocondriais / Membranas Mitocondriais Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article