Peptide, protein, and cellular interactions with self‐assembled monolayer model surfaces

S. Margel, E. A. Vogler, L. Firment, T. Watt, S. Haynie, D. Y. Sogah

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128 Scopus citations


Model biomaterial surfaces with well defined chemistry were prepared from close‐packed alkyltrichlorosilane monolayers on polished silicon and glass. The outermost molecular groups which come in direct contact with the biological environment were varied across a wide range of oxidation states by employing CF3, CH3, CO2CH3, and CH2OH terminal functionalities. Characterization by contact angles, surface spectroscopy, and ellipsometry verified that these model surfaces could be repeatedly prepared with good consistency for routine use to study biomolecule adsorption onto model surfaces. Adhesion of canine endothelial cells and the adsorption of proteins (human serum albumin and human fibrinogen) as well as a series of synthetic defined oligopeptides to these model surfaces have been studied. Endothelial cells attachment and growth were in the rank order of: CH2OH > CO2Me > CH3 > CF3. The peptides were comprised of different alternating sequences of lysine, leucine, and tryptophan residues. These structural differences imparted different amphiphilic characters that led to measurable differences in the adsorption of these peptides to liquid‐vapor interfaces. The adsorption to model surfaces was studied using ESCA, radiometry, and concentration‐dependent contact angles. ESCA and radiometry measured irreversible biomolecules adsorption whereas the contact angle method measured steadystate adsorption. Radiometric results were inconsistent with ESCA, possibly due to artifacts associated with protein radiolabeling. © 1993 John Wiley & Sons, Inc.

Original languageEnglish
Pages (from-to)1463-1476
Number of pages14
JournalJournal of Biomedical Materials Research
Issue number12
StatePublished - Dec 1993


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