In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography
The ability to produce outer membrane projections in the form of tubular membrane extensions (MEs) and membrane vesicles (MVs) is a widespread phenomenon among diderm bacteria. Despite this, our knowledge of the ultrastructure of these extensions and their associated protein complexes remains limite...
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Format: | Article |
Language: | English |
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eLife Sciences Publications Ltd
2021-09-01
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Series: | eLife |
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Online Access: | https://elifesciences.org/articles/73099 |
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doaj-9dc4069a6dfe4d3c9e60a677f0b20699 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohammed Kaplan Georges Chreifi Lauren Ann Metskas Janine Liedtke Cecily R Wood Catherine M Oikonomou William J Nicolas Poorna Subramanian Lori A Zacharoff Yuhang Wang Yi-Wei Chang Morgan Beeby Megan J Dobro Yongtao Zhu Mark J McBride Ariane Briegel Carrie L Shaffer Grant J Jensen |
spellingShingle |
Mohammed Kaplan Georges Chreifi Lauren Ann Metskas Janine Liedtke Cecily R Wood Catherine M Oikonomou William J Nicolas Poorna Subramanian Lori A Zacharoff Yuhang Wang Yi-Wei Chang Morgan Beeby Megan J Dobro Yongtao Zhu Mark J McBride Ariane Briegel Carrie L Shaffer Grant J Jensen In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography eLife cryo-ET membrane extensions tubes vesicles secretin bacteria |
author_facet |
Mohammed Kaplan Georges Chreifi Lauren Ann Metskas Janine Liedtke Cecily R Wood Catherine M Oikonomou William J Nicolas Poorna Subramanian Lori A Zacharoff Yuhang Wang Yi-Wei Chang Morgan Beeby Megan J Dobro Yongtao Zhu Mark J McBride Ariane Briegel Carrie L Shaffer Grant J Jensen |
author_sort |
Mohammed Kaplan |
title |
In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography |
title_short |
In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography |
title_full |
In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography |
title_fullStr |
In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography |
title_full_unstemmed |
In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography |
title_sort |
in situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomography |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2021-09-01 |
description |
The ability to produce outer membrane projections in the form of tubular membrane extensions (MEs) and membrane vesicles (MVs) is a widespread phenomenon among diderm bacteria. Despite this, our knowledge of the ultrastructure of these extensions and their associated protein complexes remains limited. Here, we surveyed the ultrastructure and formation of MEs and MVs, and their associated protein complexes, in tens of thousands of electron cryo-tomograms of ~90 bacterial species that we have collected for various projects over the past 15 years (Jensen lab database), in addition to data generated in the Briegel lab. We identified outer MEs and MVs in 13 diderm bacterial species and classified several major ultrastructures: (1) tubes with a uniform diameter (with or without an internal scaffold), (2) tubes with irregular diameter, (3) tubes with a vesicular dilation at their tip, (4) pearling tubes, (5) connected chains of vesicles (with or without neck-like connectors), (6) budding vesicles and nanopods. We also identified several protein complexes associated with these MEs and MVs which were distributed either randomly or exclusively at the tip. These complexes include a secretin-like structure and a novel crown-shaped structure observed primarily in vesicles from lysed cells. In total, this work helps to characterize the diversity of bacterial membrane projections and lays the groundwork for future research in this field. |
topic |
cryo-ET membrane extensions tubes vesicles secretin bacteria |
url |
https://elifesciences.org/articles/73099 |
work_keys_str_mv |
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1717373648402120704 |
spelling |
doaj-9dc4069a6dfe4d3c9e60a677f0b206992021-09-21T08:21:02ZengeLife Sciences Publications LtdeLife2050-084X2021-09-011010.7554/eLife.73099In situ imaging of bacterial outer membrane projections and associated protein complexes using electron cryo-tomographyMohammed Kaplan0https://orcid.org/0000-0002-0759-0459Georges Chreifi1https://orcid.org/0000-0003-4194-1694Lauren Ann Metskas2https://orcid.org/0000-0002-8073-6960Janine Liedtke3https://orcid.org/0000-0003-2680-4130Cecily R Wood4Catherine M Oikonomou5https://orcid.org/0000-0003-2312-4746William J Nicolas6https://orcid.org/0000-0001-5970-8626Poorna Subramanian7Lori A Zacharoff8Yuhang Wang9https://orcid.org/0000-0003-3715-8349Yi-Wei Chang10https://orcid.org/0000-0003-2391-473XMorgan Beeby11https://orcid.org/0000-0001-6413-9835Megan J Dobro12https://orcid.org/0000-0002-6464-3932Yongtao Zhu13https://orcid.org/0000-0002-3069-6518Mark J McBride14https://orcid.org/0000-0002-3798-6761Ariane Briegel15https://orcid.org/0000-0003-3733-3725Carrie L Shaffer16https://orcid.org/0000-0002-7457-7422Grant J Jensen17https://orcid.org/0000-0003-1556-4864Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesLeiden University, Sylvius Laboratories, Leiden, NetherlandsDepartment of Veterinary Science, University of Kentucky, Lexington, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesDepartment of Physics and Astronomy, University of Southern California, Los Angeles, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United StatesDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, United StatesDepartment of Life Sciences, Imperial College London, London, United KingdomHampshire College, Amherst, United StatesDepartment of Biological Sciences, Minnesota State University, Mankato, United StatesDepartment of Biological Sciences, University of Wisconsin-Milwaukee, Milwaukee, United StatesLeiden University, Sylvius Laboratories, Leiden, NetherlandsDepartment of Veterinary Science, University of Kentucky, Lexington, United States; Department of Microbiology, Immunology, and Molecular Genetics, University of Kentucky, Lexington, United States; Department of Pharmaceutical Sciences, University of Kentucky, Lexington, United StatesDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States; Department of Chemistry and Biochemistry, Brigham Young University, Provo, United StatesThe ability to produce outer membrane projections in the form of tubular membrane extensions (MEs) and membrane vesicles (MVs) is a widespread phenomenon among diderm bacteria. Despite this, our knowledge of the ultrastructure of these extensions and their associated protein complexes remains limited. Here, we surveyed the ultrastructure and formation of MEs and MVs, and their associated protein complexes, in tens of thousands of electron cryo-tomograms of ~90 bacterial species that we have collected for various projects over the past 15 years (Jensen lab database), in addition to data generated in the Briegel lab. We identified outer MEs and MVs in 13 diderm bacterial species and classified several major ultrastructures: (1) tubes with a uniform diameter (with or without an internal scaffold), (2) tubes with irregular diameter, (3) tubes with a vesicular dilation at their tip, (4) pearling tubes, (5) connected chains of vesicles (with or without neck-like connectors), (6) budding vesicles and nanopods. We also identified several protein complexes associated with these MEs and MVs which were distributed either randomly or exclusively at the tip. These complexes include a secretin-like structure and a novel crown-shaped structure observed primarily in vesicles from lysed cells. In total, this work helps to characterize the diversity of bacterial membrane projections and lays the groundwork for future research in this field.https://elifesciences.org/articles/73099cryo-ETmembrane extensionstubesvesiclessecretinbacteria |