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Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes

[Image: see text] We describe an apparatus for the cryogenic landing of particles from the ion beam of a mass spectrometer onto transmission electron microscope grids for cryo-electron microscopy. This system also allows for the controlled formation of thin films of amorphous ice on the grid surface...

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Autores principales: Westphall, Michael S., Lee, Kenneth W., Hemme, Colin, Salome, Austin Z., Mertz, Keaton, Grant, Timothy, Coon, Joshua J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568529/
https://www.ncbi.nlm.nih.gov/pubmed/37732836
http://dx.doi.org/10.1021/acs.analchem.3c03228
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author Westphall, Michael S.
Lee, Kenneth W.
Hemme, Colin
Salome, Austin Z.
Mertz, Keaton
Grant, Timothy
Coon, Joshua J.
author_facet Westphall, Michael S.
Lee, Kenneth W.
Hemme, Colin
Salome, Austin Z.
Mertz, Keaton
Grant, Timothy
Coon, Joshua J.
author_sort Westphall, Michael S.
collection PubMed
description [Image: see text] We describe an apparatus for the cryogenic landing of particles from the ion beam of a mass spectrometer onto transmission electron microscope grids for cryo-electron microscopy. This system also allows for the controlled formation of thin films of amorphous ice on the grid surface. We demonstrate that as compared to room temperature landings, the use of this cryogenic landing device greatly improves the structural preservation of deposited protein–protein complexes. Furthermore, landing under cryogenic conditions can increase the diversity of particle orientations, allowing for improved 3D structural interpretation. We conclude that this approach allows for the direct coupling of mass spectrometry with cryo-electron microscopy.
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spelling pubmed-105685292023-10-13 Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes Westphall, Michael S. Lee, Kenneth W. Hemme, Colin Salome, Austin Z. Mertz, Keaton Grant, Timothy Coon, Joshua J. Anal Chem [Image: see text] We describe an apparatus for the cryogenic landing of particles from the ion beam of a mass spectrometer onto transmission electron microscope grids for cryo-electron microscopy. This system also allows for the controlled formation of thin films of amorphous ice on the grid surface. We demonstrate that as compared to room temperature landings, the use of this cryogenic landing device greatly improves the structural preservation of deposited protein–protein complexes. Furthermore, landing under cryogenic conditions can increase the diversity of particle orientations, allowing for improved 3D structural interpretation. We conclude that this approach allows for the direct coupling of mass spectrometry with cryo-electron microscopy. American Chemical Society 2023-09-21 /pmc/articles/PMC10568529/ /pubmed/37732836 http://dx.doi.org/10.1021/acs.analchem.3c03228 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Westphall, Michael S.
Lee, Kenneth W.
Hemme, Colin
Salome, Austin Z.
Mertz, Keaton
Grant, Timothy
Coon, Joshua J.
Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes
title Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes
title_full Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes
title_fullStr Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes
title_full_unstemmed Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes
title_short Cryogenic Soft Landing Improves Structural Preservation of Protein Complexes
title_sort cryogenic soft landing improves structural preservation of protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568529/
https://www.ncbi.nlm.nih.gov/pubmed/37732836
http://dx.doi.org/10.1021/acs.analchem.3c03228
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