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Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein
[Image: see text] This paper describes a molecular strategy to restore adhesion of cells to surfaces that otherwise do not present ligands that can mediate adhesion. The approach is based on a carbonic anhydrase fusion protein that binds benzenesulfonamides and that also includes the RGD peptide mot...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907716/ https://www.ncbi.nlm.nih.gov/pubmed/20583796 http://dx.doi.org/10.1021/ja1016188 |
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author | Sánchez-Cortés, Juan Bähr, Katinka Mrksich, Milan |
author_facet | Sánchez-Cortés, Juan Bähr, Katinka Mrksich, Milan |
author_sort | Sánchez-Cortés, Juan |
collection | PubMed |
description | [Image: see text] This paper describes a molecular strategy to restore adhesion of cells to surfaces that otherwise do not present ligands that can mediate adhesion. The approach is based on a carbonic anhydrase fusion protein that binds benzenesulfonamides and that also includes the RGD peptide motif that can bind to cell-surface integrin adhesion receptors. In this way, the fusion protein can bind to a monolayer that presents the benzenesulfonamide ligand, thereby positioning the RGD peptide at the surface, where it can mediate the adhesion and spreading of cells. This strategy may provide a general method for promoting the adhesion of cells to non-natural surfaces or to defective biological matrices. |
format | Text |
id | pubmed-2907716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-29077162010-07-21 Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein Sánchez-Cortés, Juan Bähr, Katinka Mrksich, Milan J Am Chem Soc [Image: see text] This paper describes a molecular strategy to restore adhesion of cells to surfaces that otherwise do not present ligands that can mediate adhesion. The approach is based on a carbonic anhydrase fusion protein that binds benzenesulfonamides and that also includes the RGD peptide motif that can bind to cell-surface integrin adhesion receptors. In this way, the fusion protein can bind to a monolayer that presents the benzenesulfonamide ligand, thereby positioning the RGD peptide at the surface, where it can mediate the adhesion and spreading of cells. This strategy may provide a general method for promoting the adhesion of cells to non-natural surfaces or to defective biological matrices. American Chemical Society 2010-06-28 2010-07-21 /pmc/articles/PMC2907716/ /pubmed/20583796 http://dx.doi.org/10.1021/ja1016188 Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Sánchez-Cortés, Juan Bähr, Katinka Mrksich, Milan Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein |
title | Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein |
title_full | Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein |
title_fullStr | Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein |
title_full_unstemmed | Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein |
title_short | Cell Adhesion to Unnatural Ligands Mediated by a Bifunctional Protein |
title_sort | cell adhesion to unnatural ligands mediated by a bifunctional protein |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907716/ https://www.ncbi.nlm.nih.gov/pubmed/20583796 http://dx.doi.org/10.1021/ja1016188 |
work_keys_str_mv | AT sanchezcortesjuan celladhesiontounnaturalligandsmediatedbyabifunctionalprotein AT bahrkatinka celladhesiontounnaturalligandsmediatedbyabifunctionalprotein AT mrksichmilan celladhesiontounnaturalligandsmediatedbyabifunctionalprotein |