English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
Add to Basket
  Local TagsRelease HistoryDetailsSummary

Released
Journal Article

Protein repellent properties of covalently attached PEG coatings on nanostructured SiO2 based interfaces

MPS-Authors
/persons/resource/persons75300

Blümmel,  Jacques
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons75939

Perschmann,  Nadine
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;
Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany;

/persons/resource/persons75235

Aydin,  Daniel
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

/persons/resource/persons76135

Spatz,  Joachim P.
Cellular Biophysics, Max Planck Institute for Medical Research, Max Planck Society;
Biophysical Chemistry, Institute of Physical Chemistry, University of Heidelberg, 69120 Heidelberg, Germany;

External Resource

http://www.sciencedirect.com/science/article/pii/S0142961207005558/pdfft?md5=ab83c060ec6ff147decc616f961feedb&pid=1-s2.0-S0142961207005558-main.pdf
(Any fulltext)

http://dx.doi.org/10.1016/j.biomaterials.2007.07.038
(Any fulltext)

Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Blümmel, J., Perschmann, N., Aydin, D., Drinjakovic, J., Surrey, T., Lopez-Garcia, M., et al. (2007). Protein repellent properties of covalently attached PEG coatings on nanostructured SiO2 based interfaces. Biomaterials, 28(32), 4739-4747. doi:10.1016/j.biomaterials.2007.07.038.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-440A-D
Abstract
In this study, we report the systematic comparison of different poly(ethylene glycol) (PEG) self-assembled monolayers on glass with respect to their protein adsorption and cell adhesion resistance. Combining PEGylation with micellar nanolithography allowed the formation of gold nanoparticle arrays on glass and selective coverage of the free glass area by PEG. The gold nanoparticles serve as anchor points for the attachment of individual proteins and peptides such as the cell-matrix adhesion promoting cyclic RGDfK motif or the kinesin motor protein Eg5. The capability of the motor protein to bind microtubules remained unaffected by the immobilization. It was shown that the film thickness of a water swollen PEG layer is crucial to maximize the interaction between proteins and peptides with the nanostructures. Non-specific interaction between cells or microtubules and the surface was minimized. The optimum PEG layer thickness correlated with the size of gold nanoparticles which was approximately 5 nm.