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In situ structural analysis reveals membrane shape transitions during autophagosome formation

View ORCID ProfileAnna Bieber, View ORCID ProfileCristina Capitanio, View ORCID ProfilePhilipp S. Erdmann, Fabian Fiedler, Florian Beck, Chia-Wei Lee, Delong Li, View ORCID ProfileGerhard Hummer, View ORCID ProfileBrenda A. Schulman, View ORCID ProfileWolfgang Baumeister, View ORCID ProfileFlorian Wilfling
doi: https://doi.org/10.1101/2022.05.02.490291
Anna Bieber
1Max Planck Institute of Biochemistry, Molecular Structural Biology, 82152 Martinsried, Germany
2Max Planck Institute of Biochemistry, Molecular Machines and Signaling, 82152 Martinsried, Germany
3Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, MD, 20815, United States
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Cristina Capitanio
2Max Planck Institute of Biochemistry, Molecular Machines and Signaling, 82152 Martinsried, Germany
3Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, MD, 20815, United States
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Philipp S. Erdmann
1Max Planck Institute of Biochemistry, Molecular Structural Biology, 82152 Martinsried, Germany
4Human Technopole, Viale Rita Levi Montalcini, 1, 20157 Milan, Italy
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  • For correspondence: florian.wilfling@biophys.mpg.de schulman@biochem.mpg.de baumeist@biochem.mpg.de philipp.erdmann@fht.org
Fabian Fiedler
5Max Planck Institute of Biophysics, Mechanisms of Cellular Quality Control, 60439 Frankfurt a. M., Germany
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Florian Beck
1Max Planck Institute of Biochemistry, Molecular Structural Biology, 82152 Martinsried, Germany
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Chia-Wei Lee
1Max Planck Institute of Biochemistry, Molecular Structural Biology, 82152 Martinsried, Germany
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Delong Li
5Max Planck Institute of Biophysics, Mechanisms of Cellular Quality Control, 60439 Frankfurt a. M., Germany
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Gerhard Hummer
6Max Planck Institute of Biophysics, Department of Theoretical Biophysics, 60438 Frankfurt a. M., Germany
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  • ORCID record for Gerhard Hummer
Brenda A. Schulman
2Max Planck Institute of Biochemistry, Molecular Machines and Signaling, 82152 Martinsried, Germany
3Aligning Science Across Parkinson’s (ASAP) Collaborative Research Network, Chevy Chase, MD, 20815, United States
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  • For correspondence: florian.wilfling@biophys.mpg.de schulman@biochem.mpg.de baumeist@biochem.mpg.de philipp.erdmann@fht.org
Wolfgang Baumeister
1Max Planck Institute of Biochemistry, Molecular Structural Biology, 82152 Martinsried, Germany
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  • ORCID record for Wolfgang Baumeister
  • For correspondence: florian.wilfling@biophys.mpg.de schulman@biochem.mpg.de baumeist@biochem.mpg.de philipp.erdmann@fht.org
Florian Wilfling
1Max Planck Institute of Biochemistry, Molecular Structural Biology, 82152 Martinsried, Germany
2Max Planck Institute of Biochemistry, Molecular Machines and Signaling, 82152 Martinsried, Germany
5Max Planck Institute of Biophysics, Mechanisms of Cellular Quality Control, 60439 Frankfurt a. M., Germany
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  • ORCID record for Florian Wilfling
  • For correspondence: florian.wilfling@biophys.mpg.de schulman@biochem.mpg.de baumeist@biochem.mpg.de philipp.erdmann@fht.org
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Abstract

Autophagosomes are unique organelles which form de novo as double-membrane vesicles engulfing cytosolic material for destruction. Their biogenesis involves a series of membrane transformations with distinctly shaped intermediates whose ultrastructure is poorly understood. Here, we combine cell biology, correlative cryo-electron tomography (ET) and novel data analysis to reveal the step-by-step structural progression of autophagosome biogenesis at high resolution directly within yeast cells. By mapping individual structures onto a timeline based on geometric features, we uncover dynamic changes in membrane shape and curvature. Moreover, we reveal the organelle interactome of growing autophagosomes, highlighting a polar organization of contact sites between the phagophore and organelles such as the vacuole and the ER. Collectively, these findings have important implications for the contribution of different membrane sources during autophagy and for the forces shaping and driving phagophores towards closure without a templating cargo.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted May 02, 2022.
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In situ structural analysis reveals membrane shape transitions during autophagosome formation
Anna Bieber, Cristina Capitanio, Philipp S. Erdmann, Fabian Fiedler, Florian Beck, Chia-Wei Lee, Delong Li, Gerhard Hummer, Brenda A. Schulman, Wolfgang Baumeister, Florian Wilfling
bioRxiv 2022.05.02.490291; doi: https://doi.org/10.1101/2022.05.02.490291
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In situ structural analysis reveals membrane shape transitions during autophagosome formation
Anna Bieber, Cristina Capitanio, Philipp S. Erdmann, Fabian Fiedler, Florian Beck, Chia-Wei Lee, Delong Li, Gerhard Hummer, Brenda A. Schulman, Wolfgang Baumeister, Florian Wilfling
bioRxiv 2022.05.02.490291; doi: https://doi.org/10.1101/2022.05.02.490291

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