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  The structure of the COPI coat determined within the cell

Bykov, Y. S., Schaffer, M., Dodonova, S. O., Albert, S., Plitzko, J. M., Baumeister, W., et al. (2017). The structure of the COPI coat determined within the cell. eLife, e32493. doi:10.7554/eLife.32493.001.

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 Creators:
Bykov, Y. S.1, Author
Schaffer, Miroslava2, Author           
Dodonova, S. O.1, Author
Albert, Sahradha2, Author           
Plitzko, Jürgen M.2, Author           
Baumeister, Wolfgang2, Author           
Engel, Benjamin D.2, Author           
Briggs, J. A. G.1, Author
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1External Organizations, ou_persistent22              
2Baumeister, Wolfgang / Molecular Structural Biology, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565142              

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Free keywords: cryo-electron tomography, membrane trafficking, Chlamydomonas reinhardtii, COPI, subtomogram averaging
 Abstract: COPI-coated vesicles mediate trafficking within the Golgi apparatus and from the Golgi to the endoplasmic reticulum. The structures of membrane protein coats, including COPI, have been extensively studied with in vitro reconstitution systems using purified components. Previously we have determined a complete structural model of the in vitro reconstituted COPI coat (Dodonova et al., 2017). Here, we applied cryo-focused ion beam milling, cryo-electron tomography and subtomogram averaging to determine the native structure of the COPI coat within vitrified Chlamydomonas reinhardtii cells. The native algal structure resembles the in vitro mammalian structure, but additionally reveals cargo bound beneath β’–COP. We find that all coat components disassemble simultaneously and relatively rapidly after budding. Structural analysis in situ, maintaining Golgi topology, shows that vesicles change their size, membrane thickness, and cargo content as they progress from cis to trans, but the structure of the coat machinery remains constant.

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 Dates: 2017-11
 Publication Status: Published online
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 Identifiers: DOI: 10.7554/eLife.32493.001
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Project name : SFB-1035/Project A01
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Funding organization : Deutsche Forschungsgemeinschaft

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Title: eLife
Source Genre: Journal
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Publ. Info: Cambridge : eLife Sciences Publications
Pages: - Volume / Issue: - Sequence Number: e32493 Start / End Page: - Identifier: ISSN: 2050-084X
CoNE: https://pure.mpg.de/cone/journals/resource/2050-084X