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Towards Community-Driven Visual Proteomics with Large-Scale Cryo-Electron Tomography of Chlamydomonas reinhardtii

71 Pages Posted: 31 Jan 2025 Publication Status: Under Review

See all articles by Ron Kelley

Ron Kelley

Thermo Fisher Scientific

Sagar Khavnekar

Thermo Fisher Scientific

Ricardo D. Righetto

University of Basel

Jessica Heebner

Thermo Fisher Scientific

Martin Obr

Thermo Fisher Scientific

Xianjun Zhang

Thermo Fisher Scientific

Saikat Chakraborty

Thermo Fisher Scientific

Grigory Tagiltsev

Max Planck Society for the Advancement of the Sciences - Max Planck Institute of Biochemistry

Alicia K. Michael

University of Basel

Sofie van Dorst

University of Basel

Florent Waltz

University of Basel

Caitlyn L. McCafferty

University of Basel

Lorenz Lamm

University of Basel

Simon Zufferey

University of Basel

Philippe Van der Stappen

University of Basel

Hugo van den Hoek

University of Basel

Wojciech Wietrzynski

University of Basel

Pavol Harar

Institute of Science and Technology Austria (ISTA)

William Wan

Vanderbilt University

John A. G. Briggs

Max Planck Society for the Advancement of the Sciences - Max Planck Institute of Biochemistry

Jürgen M. Plitzko

Max Planck Society for the Advancement of the Sciences - Max Planck Institute of Biochemistry

Benjamin D. Engel

Max Planck Society for the Advancement of the Sciences - Department of Molecular Structural Biology

Abhay Kotecha

Thermo Fisher Scientific

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Abstract

In situ cryo-electron tomography (cryo-ET) has emerged as the method of choice to investigate structures of biomolecules in their native context. However, challenges remain in the efficient production of large-scale cryo-ET datasets, as well as the community sharing of this information-rich data. Here, we applied a cryogenic plasma-based focused ion beam (cryo-PFIB) instrument for high-throughput milling of the green alga Chlamydomonas reinhardtii, a useful model organism for in situ visualization of numerous fundamental cellular processes. Combining cryo-PFIB sample preparation with recent advances in cryo-ET data acquisition and processing, we generated a dataset of 1829 reconstructed and annotated tomograms, which we provide as a community resource to drive method development and inspire biological discovery. To assay the quality of this dataset, we performed subtomogram averaging (STA) of both soluble and membrane-bound complexes ranging in size from >3 MDa to ~200 kDa, including 80S ribosomes, Rubisco, nucleosomes, microtubules, clathrin, photosystem II, and mitochondrial ATP synthase. The majority of these density maps reached sub-nanometer resolution, demonstrating the potential of this C. reinhardtii dataset, as well as the promise of modern cryo-ET workflows and open data sharing towards visual proteomics.

Keywords: visual proteomics, focused ion beam, cryo-electron tomography, ribosome, Rubisco, nucleosome, Microtubule, clathrin, photosystem II, ATP synthase, open data

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Suggested Citation

Kelley, Ron and Khavnekar, Sagar and Righetto, Ricardo D. and Heebner, Jessica and Obr, Martin and Zhang, Xianjun and Chakraborty, Saikat and Tagiltsev, Grigory and Michael, Alicia K. and van Dorst, Sofie and Waltz, Florent and McCafferty, Caitlyn L. and Lamm, Lorenz and Zufferey, Simon and Van der Stappen, Philippe and van den Hoek, Hugo and Wietrzynski, Wojciech and Harar, Pavol and Wan, William and Briggs, John A. G. and Plitzko, Jürgen M. and Engel, Benjamin D. and Kotecha, Abhay and Administrator, Sneak Peek, Towards Community-Driven Visual Proteomics with Large-Scale Cryo-Electron Tomography of Chlamydomonas reinhardtii. Available at SSRN: https://ssrn.com/abstract=5118278 or http://dx.doi.org/10.2139/ssrn.5118278
This version of the paper has not been formally peer reviewed.

Ron Kelley

Thermo Fisher Scientific ( email )

Cambridge, OR
United Kingdom

Sagar Khavnekar

Thermo Fisher Scientific ( email )

Cambridge, OR
United Kingdom

Ricardo D. Righetto

University of Basel ( email )

Petersplatz 1
Basel, CH-4003
Switzerland

Jessica Heebner

Thermo Fisher Scientific ( email )

Cambridge, OR
United Kingdom

Martin Obr

Thermo Fisher Scientific ( email )

Cambridge, OR
United Kingdom

Xianjun Zhang

Thermo Fisher Scientific ( email )

Cambridge, OR
United Kingdom

Saikat Chakraborty

Thermo Fisher Scientific ( email )

Cambridge, OR
United Kingdom

Grigory Tagiltsev

Max Planck Society for the Advancement of the Sciences - Max Planck Institute of Biochemistry ( email )

Alicia K. Michael

University of Basel ( email )

Sofie Van Dorst

University of Basel ( email )

Florent Waltz

University of Basel ( email )

Caitlyn L. McCafferty

University of Basel ( email )

Lorenz Lamm

University of Basel ( email )

Simon Zufferey

University of Basel ( email )

Philippe Van der Stappen

University of Basel ( email )

Hugo Van den Hoek

University of Basel ( email )

Wojciech Wietrzynski

University of Basel ( email )

Petersplatz 1
Basel, CH-4003
Switzerland

Pavol Harar

Institute of Science and Technology Austria (ISTA) ( email )

Klosterneuburg, 3400
Austria

William Wan

Vanderbilt University ( email )

John A. G. Briggs

Max Planck Society for the Advancement of the Sciences - Max Planck Institute of Biochemistry ( email )

Jürgen M. Plitzko

Max Planck Society for the Advancement of the Sciences - Max Planck Institute of Biochemistry

Am Klopferspitz 18
Martinsried, 82152
Germany

Benjamin D. Engel (Contact Author)

Max Planck Society for the Advancement of the Sciences - Department of Molecular Structural Biology ( email )

Am Klopferspitz 18
Martinsried, 82152
Germany

Abhay Kotecha

Thermo Fisher Scientific ( email )

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