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Protein denaturation at the air-water interface and how to prevent it

Electron cryo-microscopy analyzes the structure of proteins and protein complexes in vitrified solution. Proteins tend to adsorb to the air-water interface in unsupported films of aqueous solution, which can result in partial or complete denaturation. We investigated the structure of yeast fatty aci...

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Autores principales: D'Imprima, Edoardo, Floris, Davide, Joppe, Mirko, Sánchez, Ricardo, Grininger, Martin, Kühlbrandt, Werner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443348/
https://www.ncbi.nlm.nih.gov/pubmed/30932812
http://dx.doi.org/10.7554/eLife.42747
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author D'Imprima, Edoardo
Floris, Davide
Joppe, Mirko
Sánchez, Ricardo
Grininger, Martin
Kühlbrandt, Werner
author_facet D'Imprima, Edoardo
Floris, Davide
Joppe, Mirko
Sánchez, Ricardo
Grininger, Martin
Kühlbrandt, Werner
author_sort D'Imprima, Edoardo
collection PubMed
description Electron cryo-microscopy analyzes the structure of proteins and protein complexes in vitrified solution. Proteins tend to adsorb to the air-water interface in unsupported films of aqueous solution, which can result in partial or complete denaturation. We investigated the structure of yeast fatty acid synthase at the air-water interface by electron cryo-tomography and single-particle image processing. Around 90% of complexes adsorbed to the air-water interface are partly denatured. We show that the unfolded regions face the air-water interface. Denaturation by contact with air may happen at any stage of specimen preparation. Denaturation at the air-water interface is completely avoided when the complex is plunge-frozen on a substrate of hydrophilized graphene.
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spelling pubmed-64433482019-04-03 Protein denaturation at the air-water interface and how to prevent it D'Imprima, Edoardo Floris, Davide Joppe, Mirko Sánchez, Ricardo Grininger, Martin Kühlbrandt, Werner eLife Structural Biology and Molecular Biophysics Electron cryo-microscopy analyzes the structure of proteins and protein complexes in vitrified solution. Proteins tend to adsorb to the air-water interface in unsupported films of aqueous solution, which can result in partial or complete denaturation. We investigated the structure of yeast fatty acid synthase at the air-water interface by electron cryo-tomography and single-particle image processing. Around 90% of complexes adsorbed to the air-water interface are partly denatured. We show that the unfolded regions face the air-water interface. Denaturation by contact with air may happen at any stage of specimen preparation. Denaturation at the air-water interface is completely avoided when the complex is plunge-frozen on a substrate of hydrophilized graphene. eLife Sciences Publications, Ltd 2019-04-01 /pmc/articles/PMC6443348/ /pubmed/30932812 http://dx.doi.org/10.7554/eLife.42747 Text en © 2019, D'Imprima et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Structural Biology and Molecular Biophysics
D'Imprima, Edoardo
Floris, Davide
Joppe, Mirko
Sánchez, Ricardo
Grininger, Martin
Kühlbrandt, Werner
Protein denaturation at the air-water interface and how to prevent it
title Protein denaturation at the air-water interface and how to prevent it
title_full Protein denaturation at the air-water interface and how to prevent it
title_fullStr Protein denaturation at the air-water interface and how to prevent it
title_full_unstemmed Protein denaturation at the air-water interface and how to prevent it
title_short Protein denaturation at the air-water interface and how to prevent it
title_sort protein denaturation at the air-water interface and how to prevent it
topic Structural Biology and Molecular Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443348/
https://www.ncbi.nlm.nih.gov/pubmed/30932812
http://dx.doi.org/10.7554/eLife.42747
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