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Structural-functional analysis of engineered protein-nanoparticle assemblies using graphene microelectrodes.
Ping, Jinglei; Pulsipher, Katherine W; Vishnubhotla, Ramya; Villegas, Jose A; Hicks, Tacey L; Honig, Stephanie; Saven, Jeffery G; Dmochowski, Ivan J; Johnson, A T Charlie.
Afiliación
  • Ping J; Department of Physics and Astronomy , University of Pennsylvania , Philadelphia , PA 19104 , USA . Email: cjohnson@physics.upenn.edu.
  • Pulsipher KW; Department of Chemistry , University of Pennsylvania , Philadelphia , PA 19104 , USA.
  • Vishnubhotla R; Department of Physics and Astronomy , University of Pennsylvania , Philadelphia , PA 19104 , USA . Email: cjohnson@physics.upenn.edu.
  • Villegas JA; Department of Chemistry , University of Pennsylvania , Philadelphia , PA 19104 , USA.
  • Hicks TL; Department of Chemistry , University of Pennsylvania , Philadelphia , PA 19104 , USA.
  • Honig S; Department of Chemistry , University of Pennsylvania , Philadelphia , PA 19104 , USA.
  • Saven JG; Department of Chemistry , University of Pennsylvania , Philadelphia , PA 19104 , USA.
  • Dmochowski IJ; Department of Chemistry , University of Pennsylvania , Philadelphia , PA 19104 , USA.
  • Johnson ATC; Department of Physics and Astronomy , University of Pennsylvania , Philadelphia , PA 19104 , USA . Email: cjohnson@physics.upenn.edu.
Chem Sci ; 8(8): 5329-5334, 2017 Aug 01.
Article en En | MEDLINE | ID: mdl-28970912
ABSTRACT
The characterization of protein-nanoparticle assemblies in solution remains a challenge. We demonstrate a technique based on a graphene microelectrode for structural-functional analysis of model systems composed of nanoparticles enclosed in open-pore and closed-pore ferritin molecules. The method readily resolves the difference in accessibility of the enclosed nanoparticle for charge transfer and offers the prospect for quantitative analysis of pore-mediated transport, while shedding light on the spatial orientation of the protein subunits on the nanoparticle surface, faster and with higher sensitivity than conventional catalysis methods.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2017 Tipo del documento: Article