Peptide interfacial biomaterials improve endothelial cell adhesion and spreading on synthetic polyglycolic acid materials.
dc.contributor.author | Huang, Xin | |
dc.contributor.author | Zauscher, Stefan | |
dc.contributor.author | Klitzman, Bruce | |
dc.contributor.author | Truskey, George A | |
dc.contributor.author | Reichert, William M | |
dc.contributor.author | Kenan, Daniel J | |
dc.contributor.author | Grinstaff, Mark W | |
dc.coverage.spatial | United States | |
dc.date.accessioned | 2015-07-30T22:57:21Z | |
dc.date.issued | 2010-06 | |
dc.description.abstract | Resorbable scaffolds such as polyglycolic acid (PGA) are employed in a number of clinical and tissue engineering applications owing to their desirable property of allowing remodeling to form native tissue over time. However, native PGA does not promote endothelial cell adhesion. Here we describe a novel treatment with hetero-bifunctional peptide linkers, termed "interfacial biomaterials" (IFBMs), which are used to alter the surface of PGA to provide appropriate biological cues. IFBMs couple an affinity peptide for the material with a biologically active peptide that promotes desired cellular responses. One such PGA affinity peptide was coupled to the integrin binding domain, Arg-Gly-Asp (RGD), to build a chemically synthesized bimodular 27 amino acid peptide that mediated interactions between PGA and integrin receptors on endothelial cells. Quartz crystal microbalance with dissipation monitoring (QCMD) was used to determine the association constant (K (A) 1 x 10(7) M(-1)) and surface thickness (~3.5 nm). Cell binding studies indicated that IFBM efficiently mediated adhesion, spreading, and cytoskeletal organization of endothelial cells on PGA in an integrin-dependent manner. We show that the IFBM peptide promotes a 200% increase in endothelial cell binding to PGA as well as 70-120% increase in cell spreading from 30 to 60 minutes after plating. | |
dc.identifier | ||
dc.identifier.eissn | 1573-9686 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.ispartof | Ann Biomed Eng | |
dc.relation.isversionof | 10.1007/s10439-010-9986-5 | |
dc.subject | Cell Adhesion | |
dc.subject | Cell Movement | |
dc.subject | Cells, Cultured | |
dc.subject | Coated Materials, Biocompatible | |
dc.subject | Endothelial Cells | |
dc.subject | Humans | |
dc.subject | Materials Testing | |
dc.subject | Oligopeptides | |
dc.subject | Polyglycolic Acid | |
dc.subject | Surface Properties | |
dc.title | Peptide interfacial biomaterials improve endothelial cell adhesion and spreading on synthetic polyglycolic acid materials. | |
dc.type | Journal article | |
duke.contributor.orcid | Zauscher, Stefan|0000-0002-2290-7178 | |
duke.contributor.orcid | Truskey, George A|0000-0002-6885-4489 | |
pubs.author-url | ||
pubs.begin-page | 1965 | |
pubs.end-page | 1976 | |
pubs.issue | 6 | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Biomedical Engineering | |
pubs.organisational-group | Cell Biology | |
pubs.organisational-group | Chemistry | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Science & Society | |
pubs.organisational-group | Initiatives | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Mechanical Engineering and Materials Science | |
pubs.organisational-group | Pratt School of Engineering | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Surgery | |
pubs.organisational-group | Surgery, Plastic, Maxillofacial, and Oral Surgery | |
pubs.organisational-group | Trinity College of Arts & Sciences | |
pubs.publication-status | Published | |
pubs.volume | 38 |
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