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  Noncovalent Functionalization of Carbon Substrates with Hydrogels Improves Structural Analysis of Vitrified Proteins by Electron Cryo-Microscopy

Scherr, J., Neuhaus, A., Parey, K., Klusch, N., Murphy, B. J., Zickermann, V., et al. (2019). Noncovalent Functionalization of Carbon Substrates with Hydrogels Improves Structural Analysis of Vitrified Proteins by Electron Cryo-Microscopy. ACS Nano, 13(6), 7185-7190. doi:10.1021/acsnano.9b02651.

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 Creators:
Scherr, Julian1, Author
Neuhaus, Alexander2, Author           
Parey, Kristian2, Author           
Klusch, Niklas2, Author                 
Murphy, Bonnie J.2, Author                 
Zickermann, Volker3, Author
Kühlbrandt, Werner2, Author                 
Terfort, Andreas1, Author
Rhinow, Daniel2, Author           
Affiliations:
1Department of Chemistry, Institute of Inorganic and Analytical Chemistry, Goethe-University Frankfurt, Frankfurt, Germany, ou_persistent22              
2Department of Structural Biology, Max Planck Institute of Biophysics, Max Planck Society, ou_2068291              
3Structural Bioenergetics Group, Institute of Biochemistry II, Medical School, Frankfurt, Germany, ou_persistent22              

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Free keywords: biorepulsive; cryo-EM; detergent; membrane protein; self-assembly
 Abstract: In electron cryo-microscopy, structure determination of protein molecules is frequently hampered by adsorption of the particles to the support film material, typically amorphous carbon. Here, we report that pyrene derivatives with one or two polyglycerol (PG) side chains bind to the amorphous carbon films, forming a biorepulsive hydrogel layer so that the number of protein particles in the vitreous ice drastically increases. This approach could be extended by adding a hydrogel-functionalized carbon nanotube network (HyCaNet, the hydrogel again being formed from the PG-pyrene derivatives), which stabilized the protein-containing thin ice films during imaging with the electron beam. The stabilization resulted in reduced particle motion by up to 70%. These substrates were instrumental for determining the structure of a large membrane protein complex.

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Language(s): eng - English
 Dates: 2019-04-062019-05-212019-05-222019-06-25
 Publication Status: Issued
 Pages: 6
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acsnano.9b02651
 Degree: -

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Title: ACS Nano
  Other : ACS Nano
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 13 (6) Sequence Number: - Start / End Page: 7185 - 7190 Identifier: ISSN: 1936-0851
CoNE: https://pure.mpg.de/cone/journals/resource/1936-0851