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Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically

The interaction of the anti-adhesive coating, poly(L-lysine)-graft-poly(ethylene glycol) (PLL-g-PEG) and its Arg-Gly-Asp (RGD) functionalized form, PLL-g-PEG-RGD, with the green tea polyphenol, epigallocatechin-gallate (EGCg) was in situ monitored. After, the kinetics of cellular adhesion on the EGC...

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Autores principales: Peter, Beatrix, Farkas, Eniko, Forgacs, Eniko, Saftics, Andras, Kovacs, Boglarka, Kurunczi, Sandor, Szekacs, Inna, Csampai, Antal, Bosze, Szilvia, Horvath, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301484/
https://www.ncbi.nlm.nih.gov/pubmed/28186133
http://dx.doi.org/10.1038/srep42220
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author Peter, Beatrix
Farkas, Eniko
Forgacs, Eniko
Saftics, Andras
Kovacs, Boglarka
Kurunczi, Sandor
Szekacs, Inna
Csampai, Antal
Bosze, Szilvia
Horvath, Robert
author_facet Peter, Beatrix
Farkas, Eniko
Forgacs, Eniko
Saftics, Andras
Kovacs, Boglarka
Kurunczi, Sandor
Szekacs, Inna
Csampai, Antal
Bosze, Szilvia
Horvath, Robert
author_sort Peter, Beatrix
collection PubMed
description The interaction of the anti-adhesive coating, poly(L-lysine)-graft-poly(ethylene glycol) (PLL-g-PEG) and its Arg-Gly-Asp (RGD) functionalized form, PLL-g-PEG-RGD, with the green tea polyphenol, epigallocatechin-gallate (EGCg) was in situ monitored. After, the kinetics of cellular adhesion on the EGCg exposed coatings were recorded in real-time. The employed plate-based waveguide biosensor is applicable to monitor small molecule binding and sensitive to sub-nanometer scale changes in cell membrane position and cell mass distribution; while detecting the signals of thousands of adhering cells. The combination of this remarkable sensitivity and throughput opens up new avenues in testing complicated models of cell-surface interactions. The systematic studies revealed that, despite the reported excellent antifouling properties of the coatings, EGCg strongly interacted with them, and affected their cell adhesivity in a concentration dependent manner. Moreover, the differences between the effects of the fresh and oxidized EGCg solutions were first demonstrated. Using a semiempirical quantumchemical method we showed that EGCg binds to the PEG chains of PLL-g-PEG-RGD and effectively blocks the RGD sites by hydrogen bonds. The calculations supported the experimental finding that the binding is stronger for the oxidative products. Our work lead to a new model of polyphenol action on cell adhesion ligand accessibility and matrix rigidity.
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spelling pubmed-53014842017-02-15 Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically Peter, Beatrix Farkas, Eniko Forgacs, Eniko Saftics, Andras Kovacs, Boglarka Kurunczi, Sandor Szekacs, Inna Csampai, Antal Bosze, Szilvia Horvath, Robert Sci Rep Article The interaction of the anti-adhesive coating, poly(L-lysine)-graft-poly(ethylene glycol) (PLL-g-PEG) and its Arg-Gly-Asp (RGD) functionalized form, PLL-g-PEG-RGD, with the green tea polyphenol, epigallocatechin-gallate (EGCg) was in situ monitored. After, the kinetics of cellular adhesion on the EGCg exposed coatings were recorded in real-time. The employed plate-based waveguide biosensor is applicable to monitor small molecule binding and sensitive to sub-nanometer scale changes in cell membrane position and cell mass distribution; while detecting the signals of thousands of adhering cells. The combination of this remarkable sensitivity and throughput opens up new avenues in testing complicated models of cell-surface interactions. The systematic studies revealed that, despite the reported excellent antifouling properties of the coatings, EGCg strongly interacted with them, and affected their cell adhesivity in a concentration dependent manner. Moreover, the differences between the effects of the fresh and oxidized EGCg solutions were first demonstrated. Using a semiempirical quantumchemical method we showed that EGCg binds to the PEG chains of PLL-g-PEG-RGD and effectively blocks the RGD sites by hydrogen bonds. The calculations supported the experimental finding that the binding is stronger for the oxidative products. Our work lead to a new model of polyphenol action on cell adhesion ligand accessibility and matrix rigidity. Nature Publishing Group 2017-02-10 /pmc/articles/PMC5301484/ /pubmed/28186133 http://dx.doi.org/10.1038/srep42220 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Peter, Beatrix
Farkas, Eniko
Forgacs, Eniko
Saftics, Andras
Kovacs, Boglarka
Kurunczi, Sandor
Szekacs, Inna
Csampai, Antal
Bosze, Szilvia
Horvath, Robert
Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically
title Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically
title_full Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically
title_fullStr Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically
title_full_unstemmed Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically
title_short Green tea polyphenol tailors cell adhesivity of RGD displaying surfaces: multicomponent models monitored optically
title_sort green tea polyphenol tailors cell adhesivity of rgd displaying surfaces: multicomponent models monitored optically
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5301484/
https://www.ncbi.nlm.nih.gov/pubmed/28186133
http://dx.doi.org/10.1038/srep42220
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