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Cell patterning via linker-free protein functionalization of an organic conducting polymer (polypyrrole) electrode.

Authors :
Bax DV
Tipa RS
Kondyurin A
Higgins MJ
Tsoutas K
Gelmi A
Wallace GG
McKenzie DR
Weiss AS
Bilek MM
Source :
Acta biomaterialia [Acta Biomater] 2012 Jul; Vol. 8 (7), pp. 2538-48. Date of Electronic Publication: 2012 Mar 16.
Publication Year :
2012

Abstract

The interaction of proteins and cells with polymers is critical to their use in scientific and medical applications. In this study, plasma immersion ion implantation (PIII) was used to modify the surface of the conducting polymer, polypyrrole, which possesses electrical properties. PIII treatment enabled persistent, covalent binding of the cell adhesive protein, tropoelastin, without employing chemical linking molecules. In contrast tropoelastin was readily eluted from the untreated surface. Through this differential persistence of binding, surface bound tropoelastin supported cell adhesion and spreading on the PIII treated but not the untreated polypyrrole surface. The application of a steel shadow mask during PIII treatment allowed for spatial definition of tropoelastin exclusively to PIII treated regions. The general applicability of this approach to other extracellular matrix proteins was illustrated using collagen I, which displayed similar results to tropoelastin but required extended washing conditions. This approach allowed fine patterning of cell adhesion and spreading to tropoelastin and collagen, specifically on PIII treated polypyrrole regions. We therefore present a methodology to alter the functionality of polypyrrole surfaces, generating surfaces that can spatially control cellular interactions through protein functionalization with the potential for electrical stimulation.<br /> (Copyright © 2012 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1878-7568
Volume :
8
Issue :
7
Database :
MEDLINE
Journal :
Acta biomaterialia
Publication Type :
Academic Journal
Accession number :
22426287
Full Text :
https://doi.org/10.1016/j.actbio.2012.03.023