Source:http://linkedlifedata.com/resource/pubmed/id/11587038
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2001-10-5
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pubmed:abstractText |
In this study we present methods to physico-chemically modify micropatterned cell culture substrates that were manufactured using plasma lithography to incorporate affinity structures for specific cell binding. The surfaces consist of a pattern of a fluorocarbon plasma polymer with feature sizes between 5 and 100 microm on a background of a non-fouling tetraglyme (tetraethylene glycol dimethyl ether) plasma polymer. The tetraglyme polymer blocks virtually all non-specific binding of proteins, and it is non-adhesive for a fluorocarbon-polyethylene glycol (FC-PEG) surfactant designed to act as a 'hydrophobic anchor' for peptides. The surfactant shows a strong affinity for the fluorocarbon polymer pattern, thus enabling us to form a pattern of the surfactant-conjugated peptide. To verify this, we have synthesized a conjugate between histamine (as a model for a more complex peptide) and a commercially available FC-PEG surfactant. Disuccinimidyl carbonate was used to activate the terminal -OH group of the polyethylene glycol headgroup for the reaction with the amine-containing molecule. Affinity pattern formation can easily be achieved by immersion of the patterned substrates in a solution of the peptide-surfactant conjugate. Time of flight secondary ion mass spectroscopy in the imaging mode was used to verify that the surfactant localizes on the pattern, while the background remains bare. A model protein, bovine serum albumin, showed the same behavior. This suggests that these surfaces can be used for the formation of patterns of cell-adhesive proteins. These substrates will be used to investigate the influence of the cell size and shape of vascular smooth muscle cells on their physiology.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Ethylene Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorocarbon Polymers,
http://linkedlifedata.com/resource/pubmed/chemical/Histamine,
http://linkedlifedata.com/resource/pubmed/chemical/Polyethylene Glycols,
http://linkedlifedata.com/resource/pubmed/chemical/Serum Albumin, Bovine,
http://linkedlifedata.com/resource/pubmed/chemical/tetraglyme
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pubmed:status |
MEDLINE
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pubmed:issn |
0920-5063
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
739-53
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pubmed:dateRevised |
2008-2-20
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pubmed:meshHeading |
pubmed-meshheading:11587038-Adsorption,
pubmed-meshheading:11587038-Animals,
pubmed-meshheading:11587038-Biocompatible Materials,
pubmed-meshheading:11587038-Biomedical Engineering,
pubmed-meshheading:11587038-Cattle,
pubmed-meshheading:11587038-Ethylene Glycols,
pubmed-meshheading:11587038-Fluorocarbon Polymers,
pubmed-meshheading:11587038-Histamine,
pubmed-meshheading:11587038-Microscopy, Atomic Force,
pubmed-meshheading:11587038-Polyethylene Glycols,
pubmed-meshheading:11587038-Protein Binding,
pubmed-meshheading:11587038-Serum Albumin, Bovine,
pubmed-meshheading:11587038-Spectrometry, Mass, Secondary Ion,
pubmed-meshheading:11587038-Spectrum Analysis,
pubmed-meshheading:11587038-Surface Properties
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pubmed:year |
2001
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pubmed:articleTitle |
Plasma lithography--thin-film patterning of polymers by RF plasma polymerization II: Study of differential binding using adsorption probes.
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pubmed:affiliation |
Department of Bioengineering. University of Washington, Seattle 98195, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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