Author
Listed:
- Basil J. Greber
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
- Daniel Boehringer
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
- Alexander Leitner
(Institute of Molecular Systems Biology, Wolfgang-Pauli-Strasse 16, ETH Zurich, CH-8093 Zurich, Switzerland)
- Philipp Bieri
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
- Felix Voigts-Hoffmann
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
- Jan P. Erzberger
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
- Marc Leibundgut
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
- Ruedi Aebersold
(Institute of Molecular Systems Biology, Wolfgang-Pauli-Strasse 16, ETH Zurich, CH-8093 Zurich, Switzerland
Faculty of Science, University of Zurich, CH-8057 Zurich, Switzerland)
- Nenad Ban
(Institute of Molecular Biology and Biophysics, Schafmattstrasse 20, ETH Zurich, CH-8093 Zurich, Switzerland)
Abstract
Mitochondrial ribosomes synthesize a number of highly hydrophobic proteins encoded on the genome of mitochondria, the organelles in eukaryotic cells that are responsible for energy conversion by oxidative phosphorylation. The ribosomes in mammalian mitochondria have undergone massive structural changes throughout their evolution, including ribosomal RNA shortening and acquisition of mitochondria-specific ribosomal proteins. Here we present the three-dimensional structure of the 39S large subunit of the porcine mitochondrial ribosome determined by cryo-electron microscopy at 4.9 Å resolution. The structure, combined with data from chemical crosslinking and mass spectrometry experiments, reveals the unique features of the 39S subunit at near-atomic resolution and provides detailed insight into the architecture of the polypeptide exit site. This region of the mitochondrial ribosome has been considerably remodelled compared to its bacterial counterpart, providing a specialized platform for the synthesis and membrane insertion of the highly hydrophobic protein components of the respiratory chain.
Suggested Citation
Basil J. Greber & Daniel Boehringer & Alexander Leitner & Philipp Bieri & Felix Voigts-Hoffmann & Jan P. Erzberger & Marc Leibundgut & Ruedi Aebersold & Nenad Ban, 2014.
"Architecture of the large subunit of the mammalian mitochondrial ribosome,"
Nature, Nature, vol. 505(7484), pages 515-519, January.
Handle:
RePEc:nat:nature:v:505:y:2014:i:7484:d:10.1038_nature12890
DOI: 10.1038/nature12890
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