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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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Scherr, Julian1, Autor
Neuhaus, Alexander2, Autor           
Parey, Kristian2, Autor           
Klusch, Niklas2, Autor                 
Murphy, Bonnie J.2, Autor                 
Zickermann, Volker3, Autor
Kühlbrandt, Werner2, Autor                 
Terfort, Andreas1, Autor
Rhinow, Daniel2, Autor           
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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Schlagwörter: biorepulsive; cryo-EM; detergent; membrane protein; self-assembly
 Zusammenfassung: 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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Sprache(n): eng - English
 Datum: 2019-04-062019-05-212019-05-222019-06-25
 Publikationsstatus: Erschienen
 Seiten: 6
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1021/acsnano.9b02651
 Art des Abschluß: -

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Titel: ACS Nano
  Andere : ACS Nano
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Washington, DC : American Chemical Society
Seiten: - Band / Heft: 13 (6) Artikelnummer: - Start- / Endseite: 7185 - 7190 Identifikator: ISSN: 1936-0851
CoNE: https://pure.mpg.de/cone/journals/resource/1936-0851