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Surface Coating Structure and Its Interaction with Cytochrome in EG-Coated Nanoparticles Varies with Surface Curvature.

作者信息

Daly Clyde A, Allen Caley, Rozanov Nikita, Chong Gene, Melby Eric S, Kuech Thomas R, Lohse Samuel E, Murphy Catherine J, Pedersen Joel A, Hernandez Rigoberto

机构信息

Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States.

Environmental Chemistry and Technology Program, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.

出版信息

Langmuir. 2020 May 12;36(18):5030-5039. doi: 10.1021/acs.langmuir.0c00681. Epub 2020 Apr 29.

Abstract

The composition, orientation, and conformation of proteins in biomolecular coronas acquired by nanoparticles in biological media contribute to how they are identified by a cell. While numerous studies have investigated protein composition in biomolecular coronas, relatively little detail is known about how the nanoparticle surface influences the orientation and conformation of the proteins associated with them. We previously showed that the peripheral membrane protein cytochrome adopts preferred poses relative to negatively charged 3-mercaptopropionic acid (MPA)-gold nanoparticles (AuNPs). Here, we employ molecular dynamics simulations and complementary experiments to establish that cytochrome also assumes preferred poses upon association with nanoparticles functionalized with an uncharged ligand, specifically ω-(1-mercaptounde-11-cyl)hexa(ethylene glycol) (EG). We find that the display of the EG ligands is sensitive to the curvature of the surface-and, consequently, the effective diameter of the nearly spherical nanoparticle core-which in turn affects the preferred poses of cytochrome .

摘要

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