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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...

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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
Descripción
Sumario:[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.