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Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings
Neural prosthetic implants are currently being developed for the treatment and study of both peripheral and central nervous system disorders. Effective integration of these devices upon implantation is a critical hurdle to achieving function. As a result, much attention has been directed towards the...
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Formato: | Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701681/ https://www.ncbi.nlm.nih.gov/pubmed/19562090 http://dx.doi.org/10.3389/neuro.16.009.2009 |
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author | Straley, Karin S. Heilshorn, Sarah C. |
author_facet | Straley, Karin S. Heilshorn, Sarah C. |
author_sort | Straley, Karin S. |
collection | PubMed |
description | Neural prosthetic implants are currently being developed for the treatment and study of both peripheral and central nervous system disorders. Effective integration of these devices upon implantation is a critical hurdle to achieving function. As a result, much attention has been directed towards the development of biocompatible coatings that prolong their in vivo lifespan. In this work, we present a novel approach to fabricate such coatings, which specifically involves the use of surface-adsorbed, nanoscale-designed protein polymers to prepare reproducible, customized surfaces. A nanoscale modular design strategy was employed to synthesize six engineered, recombinant proteins intended to mimic aspects of the extracellular matrix proteins fibronectin, laminin, and elastin as well as the cell–cell adhesive protein neural cell adhesion molecule. Physical adsorption isotherms were experimentally determined for these engineered proteins, allowing for direct calculation of the available ligand density present on coated surfaces. As confirmation that ligand density in these engineered systems impacts neuronal cell behavior, we demonstrate that increasing the density of fibronectin-derived RGD ligands on coated surfaces while maintaining uniform protein surface coverage results in enhanced neurite extension of PC-12 cells. Therefore, this engineered protein adsorption approach allows for the facile preparation of tunable, quantifiable, and reproducible surfaces for in vitro studies of cell–ligand interactions and for potential application as coatings on neural implants. |
format | Text |
id | pubmed-2701681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-27016812009-06-26 Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings Straley, Karin S. Heilshorn, Sarah C. Front Neuroengineering Neuroscience Neural prosthetic implants are currently being developed for the treatment and study of both peripheral and central nervous system disorders. Effective integration of these devices upon implantation is a critical hurdle to achieving function. As a result, much attention has been directed towards the development of biocompatible coatings that prolong their in vivo lifespan. In this work, we present a novel approach to fabricate such coatings, which specifically involves the use of surface-adsorbed, nanoscale-designed protein polymers to prepare reproducible, customized surfaces. A nanoscale modular design strategy was employed to synthesize six engineered, recombinant proteins intended to mimic aspects of the extracellular matrix proteins fibronectin, laminin, and elastin as well as the cell–cell adhesive protein neural cell adhesion molecule. Physical adsorption isotherms were experimentally determined for these engineered proteins, allowing for direct calculation of the available ligand density present on coated surfaces. As confirmation that ligand density in these engineered systems impacts neuronal cell behavior, we demonstrate that increasing the density of fibronectin-derived RGD ligands on coated surfaces while maintaining uniform protein surface coverage results in enhanced neurite extension of PC-12 cells. Therefore, this engineered protein adsorption approach allows for the facile preparation of tunable, quantifiable, and reproducible surfaces for in vitro studies of cell–ligand interactions and for potential application as coatings on neural implants. Frontiers Research Foundation 2009-06-18 /pmc/articles/PMC2701681/ /pubmed/19562090 http://dx.doi.org/10.3389/neuro.16.009.2009 Text en Copyright © 2009 Straley and Heilshorn. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited. |
spellingShingle | Neuroscience Straley, Karin S. Heilshorn, Sarah C. Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings |
title | Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings |
title_full | Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings |
title_fullStr | Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings |
title_full_unstemmed | Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings |
title_short | Design and Adsorption of Modular Engineered Proteins to Prepare Customized, Neuron-Compatible Coatings |
title_sort | design and adsorption of modular engineered proteins to prepare customized, neuron-compatible coatings |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2701681/ https://www.ncbi.nlm.nih.gov/pubmed/19562090 http://dx.doi.org/10.3389/neuro.16.009.2009 |
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