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The effect of the serum corona on interactions between a single nano-object and a living cell.
Dror, Yael; Sorkin, Raya; Brand, Guy; Boubriak, Olga; Urban, Jill; Klein, Jacob.
Afiliación
  • Dror Y; Materials and Interfaces Department, Weizmann Institute of Science, Rehovot 76100, Israel.
  • Sorkin R; Department of Physical and Theoretical Chemistry, Oxford University, Oxford OX1 3QZ, United Kingdom.
  • Brand G; Materials and Interfaces Department, Weizmann Institute of Science, Rehovot 76100, Israel.
  • Boubriak O; Materials and Interfaces Department, Weizmann Institute of Science, Rehovot 76100, Israel.
  • Urban J; University Laboratory of Physiology, Oxford University, Parks Road, Oxford OX1 3PT, United Kingdom.
  • Klein J; University Laboratory of Physiology, Oxford University, Parks Road, Oxford OX1 3PT, United Kingdom.
Sci Rep ; 7: 45758, 2017 04 06.
Article en En | MEDLINE | ID: mdl-28383528
ABSTRACT
Nanoparticles (NPs) which enter physiological fluids are rapidly coated by proteins, forming a so-called corona which may strongly modify their interaction with tissues and cells relative to the bare NPs. In this work the interactions between a living cell and a nano-object, and in particular the effect on this of the adsorption of serum proteins, are directly examined by measuring the forces arising as an Atomic Force Microscope tip (diameter 20 nm) - simulating a nano-object - approaches and contacts a cell. We find that the presence of a serum protein corona on the tip strongly modifies the interaction as indicated by pronounced increase in the indentation, hysteresis and work of adhesion compared to a bare tip. Classically one expects an AFM tip interacting with a cell surface to be repelled due to cell elastic distortion, offset by tip-cell adhesion, and indeed such a model fits the bare-tip/cell interaction, in agreement with earlier work. However, the force plots obtained with serum-modified tips are very different, indicating that the cell is much more compliant to the approaching tip. The insights obtained in this work may promote better design of NPs for drug delivery and other nano-medical applications.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Sanguíneas / Nanopartículas / Fibroblastos Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Sanguíneas / Nanopartículas / Fibroblastos Límite: Animals Idioma: En Revista: Sci Rep Año: 2017 Tipo del documento: Article País de afiliación: Israel