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Self-Assembly of RGD-Functionalized Recombinant Spider Silk Protein into Microspheres in Physiological Buffer and in the Presence of Hyaluronic Acid
[Image: see text] Biomaterials made of self-assembling protein building blocks are widely explored for biomedical applications, for example, as drug carriers, tissue engineering scaffolds, and functionalized coatings. It has previously been shown that a recombinant spider silk protein functionalized...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521021/ https://www.ncbi.nlm.nih.gov/pubmed/37579070 http://dx.doi.org/10.1021/acsabm.3c00373 |
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author | Ornithopoulou, Eirini Åstrand, Carolina Gustafsson, Linnea Crouzier, Thomas Hedhammar, My |
author_facet | Ornithopoulou, Eirini Åstrand, Carolina Gustafsson, Linnea Crouzier, Thomas Hedhammar, My |
author_sort | Ornithopoulou, Eirini |
collection | PubMed |
description | [Image: see text] Biomaterials made of self-assembling protein building blocks are widely explored for biomedical applications, for example, as drug carriers, tissue engineering scaffolds, and functionalized coatings. It has previously been shown that a recombinant spider silk protein functionalized with a cell binding motif from fibronectin, FN-4RepCT (FN-silk), self-assembles into fibrillar structures at interfaces, i.e., membranes, fibers, or foams at liquid/air interfaces, and fibrillar coatings at liquid/solid interfaces. Recently, we observed that FN-silk also assembles into microspheres in the bulk of a physiological buffer (PBS) solution. Herein, we investigate the self-assembly process of FN-silk into microspheres in the bulk and how its progression is affected by the presence of hyaluronic acid (HA), both in solution and in a cross-linked HA hydrogel. Moreover, we characterize the size, morphology, mesostructure, and protein secondary structure of the FN-silk microspheres prepared in PBS and HA. Finally, we examine how the FN-silk microspheres can be used to mediate cell adhesion and spreading of human mesenchymal stem cells (hMSCs) during cell culture. These investigations contribute to our fundamental understanding of the self-assembly of silk protein into materials and demonstrate the use of silk microspheres as additives for cell culture applications. |
format | Online Article Text |
id | pubmed-10521021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-105210212023-09-27 Self-Assembly of RGD-Functionalized Recombinant Spider Silk Protein into Microspheres in Physiological Buffer and in the Presence of Hyaluronic Acid Ornithopoulou, Eirini Åstrand, Carolina Gustafsson, Linnea Crouzier, Thomas Hedhammar, My ACS Appl Bio Mater [Image: see text] Biomaterials made of self-assembling protein building blocks are widely explored for biomedical applications, for example, as drug carriers, tissue engineering scaffolds, and functionalized coatings. It has previously been shown that a recombinant spider silk protein functionalized with a cell binding motif from fibronectin, FN-4RepCT (FN-silk), self-assembles into fibrillar structures at interfaces, i.e., membranes, fibers, or foams at liquid/air interfaces, and fibrillar coatings at liquid/solid interfaces. Recently, we observed that FN-silk also assembles into microspheres in the bulk of a physiological buffer (PBS) solution. Herein, we investigate the self-assembly process of FN-silk into microspheres in the bulk and how its progression is affected by the presence of hyaluronic acid (HA), both in solution and in a cross-linked HA hydrogel. Moreover, we characterize the size, morphology, mesostructure, and protein secondary structure of the FN-silk microspheres prepared in PBS and HA. Finally, we examine how the FN-silk microspheres can be used to mediate cell adhesion and spreading of human mesenchymal stem cells (hMSCs) during cell culture. These investigations contribute to our fundamental understanding of the self-assembly of silk protein into materials and demonstrate the use of silk microspheres as additives for cell culture applications. American Chemical Society 2023-08-14 /pmc/articles/PMC10521021/ /pubmed/37579070 http://dx.doi.org/10.1021/acsabm.3c00373 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ornithopoulou, Eirini Åstrand, Carolina Gustafsson, Linnea Crouzier, Thomas Hedhammar, My Self-Assembly of RGD-Functionalized Recombinant Spider Silk Protein into Microspheres in Physiological Buffer and in the Presence of Hyaluronic Acid |
title | Self-Assembly of
RGD-Functionalized Recombinant Spider
Silk Protein into Microspheres in Physiological Buffer and in the
Presence of Hyaluronic Acid |
title_full | Self-Assembly of
RGD-Functionalized Recombinant Spider
Silk Protein into Microspheres in Physiological Buffer and in the
Presence of Hyaluronic Acid |
title_fullStr | Self-Assembly of
RGD-Functionalized Recombinant Spider
Silk Protein into Microspheres in Physiological Buffer and in the
Presence of Hyaluronic Acid |
title_full_unstemmed | Self-Assembly of
RGD-Functionalized Recombinant Spider
Silk Protein into Microspheres in Physiological Buffer and in the
Presence of Hyaluronic Acid |
title_short | Self-Assembly of
RGD-Functionalized Recombinant Spider
Silk Protein into Microspheres in Physiological Buffer and in the
Presence of Hyaluronic Acid |
title_sort | self-assembly of
rgd-functionalized recombinant spider
silk protein into microspheres in physiological buffer and in the
presence of hyaluronic acid |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521021/ https://www.ncbi.nlm.nih.gov/pubmed/37579070 http://dx.doi.org/10.1021/acsabm.3c00373 |
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