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


ABSTRACT: 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.

SUBMITTER: D'Imprima E 

PROVIDER: S-EPMC6443348 | biostudies-literature | 2019 Apr

REPOSITORIES: biostudies-literature

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

D'Imprima Edoardo E   Floris Davide D   Joppe Mirko M   Sánchez Ricardo R   Grininger Martin M   Kühlbrandt Werner W  

eLife 20190401


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 t  ...[more]

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