Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Sánchez-Cortés, Juan, Bähr, Katinka, Mrksich, Milan
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2010
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
_version_ 1782184135032307712
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