Literature DB >> 18314738

Studying proteolysis within mitochondria.

Takashi Tatsuta1, Thomas Langer.   

Abstract

Mitochondria are dynamic organelles with activities that adjust to altering physiological conditions and variable metabolic demands. A conserved proteolytic system present within the organelle exerts essential functions during the biogenesis of mitochondria and ensures the maintenance of organellar activities under varying conditions. Proteases dependent on adenosine triphosphate, in concert with oligopeptidases, degrade nonassembled or damaged proteins in various subcompartments of mitochondria, preventing their accumulation and possibly deleterious effects on mitochondrial functions. Although an increasing number of mitochondrial peptidases are characterized and functionally linked to diverse cellular processes, only limited information is available on the stability of the mitochondrial proteome and the turnover rates of individual proteins. We describe experimental approaches in the yeast Saccharomyces cerevisiae and in mice, allowing analysis of the proteolytic breakdown of mitochondrial proteins individually or on a proteomewide scale.

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Year:  2007        PMID: 18314738     DOI: 10.1007/978-1-59745-365-3_25

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  13 in total

1.  m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria.

Authors:  Takashi Tatsuta; Steffen Augustin; Mark Nolden; Björn Friedrichs; Thomas Langer
Journal:  EMBO J       Date:  2007-01-24       Impact factor: 11.598

2.  Substrate recognition by AAA+ ATPases: distinct substrate binding modes in ATP-dependent protease Yme1 of the mitochondrial intermembrane space.

Authors:  Martin Graef; Georgeta Seewald; Thomas Langer
Journal:  Mol Cell Biol       Date:  2007-01-29       Impact factor: 4.272

Review 3.  Mitochondrial protein quality control in health and disease.

Authors:  Michael J Baker; Catherine S Palmer; Diana Stojanovski
Journal:  Br J Pharmacol       Date:  2014-04       Impact factor: 8.739

4.  Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria.

Authors:  Florian Bonn; Takashi Tatsuta; Carmelina Petrungaro; Jan Riemer; Thomas Langer
Journal:  EMBO J       Date:  2011-05-24       Impact factor: 11.598

5.  Regulation of mitochondrial phospholipids by Ups1/PRELI-like proteins depends on proteolysis and Mdm35.

Authors:  Christoph Potting; Claudia Wilmes; Tanja Engmann; Christof Osman; Thomas Langer
Journal:  EMBO J       Date:  2010-07-23       Impact factor: 11.598

6.  Prohibitins interact genetically with Atp23, a novel processing peptidase and chaperone for the F1Fo-ATP synthase.

Authors:  Christof Osman; Claudia Wilmes; Takashi Tatsuta; Thomas Langer
Journal:  Mol Biol Cell       Date:  2006-11-29       Impact factor: 4.138

7.  Autocatalytic processing of m-AAA protease subunits in mitochondria.

Authors:  Mirko Koppen; Florian Bonn; Sarah Ehses; Thomas Langer
Journal:  Mol Biol Cell       Date:  2009-08-05       Impact factor: 4.138

8.  Lack of FTSH4 Protease Affects Protein Carbonylation, Mitochondrial Morphology, and Phospholipid Content in Mitochondria of Arabidopsis: New Insights into a Complex Interplay.

Authors:  Elwira Smakowska; Renata Skibior-Blaszczyk; Malgorzata Czarna; Marta Kolodziejczak; Malgorzata Kwasniak-Owczarek; Katarzyna Parys; Christiane Funk; Hanna Janska
Journal:  Plant Physiol       Date:  2016-06-13       Impact factor: 8.340

9.  Metallation state of human manganese superoxide dismutase expressed in Saccharomyces cerevisiae.

Authors:  Mei M Whittaker; James W Whittaker
Journal:  Arch Biochem Biophys       Date:  2012-04-26       Impact factor: 4.013

10.  An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases.

Authors:  Steffen Augustin; Florian Gerdes; Sukyeong Lee; Francis T F Tsai; Thomas Langer; Takashi Tatsuta
Journal:  Mol Cell       Date:  2009-09-11       Impact factor: 17.970

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