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Optimizing the Performance of Supported Lipid Bilayers as Cell Culture Platforms Based on Extracellular Matrix Functionalization
[Image: see text] Strategies to fabricate biofunctionalized surfaces are essential for many biotechnological applications. Zwitterionic lipid bilayer coatings doped with lipids with chemically selective headgroups provide a robust platform for immobilization of biomolecules in an antifouling, protei...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044817/ https://www.ncbi.nlm.nih.gov/pubmed/30023663 http://dx.doi.org/10.1021/acsomega.7b00158 |
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author | Vafaei, Setareh Tabaei, Seyed R. Cho, Nam-Joon |
author_facet | Vafaei, Setareh Tabaei, Seyed R. Cho, Nam-Joon |
author_sort | Vafaei, Setareh |
collection | PubMed |
description | [Image: see text] Strategies to fabricate biofunctionalized surfaces are essential for many biotechnological applications. Zwitterionic lipid bilayer coatings doped with lipids with chemically selective headgroups provide a robust platform for immobilization of biomolecules in an antifouling, protein resistant background. Herein, we assess the biological activity of two important components of the extracellular matrix (ECM), collagen type I (Col I) and fibronectin (FN), which are covalently attached to a supported lipid bilayer (SLB), and compare their activity with the same proteins, nonspecifically adsorbed onto a SiO(2) surface. The characterization of protein coatings by quartz crystal microbalance with dissipation revealed that Col I and FN attached to SLB are less dense and have higher structural flexibility than when adsorbed onto SiO(2). Cell adhesion, proliferation, and function, as well as Col I–FN interactions, were more efficient on the ECM-functionalized SLB, making it a promising platform for cell-based diagnostics, tissue engineering, medical implants, and biosensor development. |
format | Online Article Text |
id | pubmed-6044817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60448172018-07-16 Optimizing the Performance of Supported Lipid Bilayers as Cell Culture Platforms Based on Extracellular Matrix Functionalization Vafaei, Setareh Tabaei, Seyed R. Cho, Nam-Joon ACS Omega [Image: see text] Strategies to fabricate biofunctionalized surfaces are essential for many biotechnological applications. Zwitterionic lipid bilayer coatings doped with lipids with chemically selective headgroups provide a robust platform for immobilization of biomolecules in an antifouling, protein resistant background. Herein, we assess the biological activity of two important components of the extracellular matrix (ECM), collagen type I (Col I) and fibronectin (FN), which are covalently attached to a supported lipid bilayer (SLB), and compare their activity with the same proteins, nonspecifically adsorbed onto a SiO(2) surface. The characterization of protein coatings by quartz crystal microbalance with dissipation revealed that Col I and FN attached to SLB are less dense and have higher structural flexibility than when adsorbed onto SiO(2). Cell adhesion, proliferation, and function, as well as Col I–FN interactions, were more efficient on the ECM-functionalized SLB, making it a promising platform for cell-based diagnostics, tissue engineering, medical implants, and biosensor development. American Chemical Society 2017-06-01 /pmc/articles/PMC6044817/ /pubmed/30023663 http://dx.doi.org/10.1021/acsomega.7b00158 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Vafaei, Setareh Tabaei, Seyed R. Cho, Nam-Joon Optimizing the Performance of Supported Lipid Bilayers as Cell Culture Platforms Based on Extracellular Matrix Functionalization |
title | Optimizing the Performance of Supported Lipid Bilayers
as Cell Culture Platforms Based on Extracellular Matrix Functionalization |
title_full | Optimizing the Performance of Supported Lipid Bilayers
as Cell Culture Platforms Based on Extracellular Matrix Functionalization |
title_fullStr | Optimizing the Performance of Supported Lipid Bilayers
as Cell Culture Platforms Based on Extracellular Matrix Functionalization |
title_full_unstemmed | Optimizing the Performance of Supported Lipid Bilayers
as Cell Culture Platforms Based on Extracellular Matrix Functionalization |
title_short | Optimizing the Performance of Supported Lipid Bilayers
as Cell Culture Platforms Based on Extracellular Matrix Functionalization |
title_sort | optimizing the performance of supported lipid bilayers
as cell culture platforms based on extracellular matrix functionalization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044817/ https://www.ncbi.nlm.nih.gov/pubmed/30023663 http://dx.doi.org/10.1021/acsomega.7b00158 |
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