Peptide-PEG amphiphiles as cytophobic coatings for mammalian and bacterial cells

被引:29
作者
Kenan, Daniel J. [1 ]
Walsh, Elisabeth B.
Meyers, Steven R.
O'Toole, George A.
Carruthers, Erin G.
Lee, Woo K.
Zauscher, Stefan
Prata, Carla A. H.
Grinstaff, Mark W.
机构
[1] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[2] Duke Univ, Dept Chem, Durham, NC 27710 USA
[3] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[4] Boston Univ, Dept Chem, Boston, MA 02215 USA
[5] Dartmouth Med Sch, Dept Microbiol & Immunol, Hanover, NH 03755 USA
[6] Duke Univ, Dept Mech Engn, Durham, NC 27708 USA
[7] Duke Univ, Dept Mat Sci, Durham, NC 27708 USA
来源
CHEMISTRY & BIOLOGY | 2006年 / 13卷 / 07期
关键词
D O I
10.1016/j.chembiol.2006.06.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amphiphilic macromolecules containing a polystyrene-adherent peptide domain and a cell-repellent poly(ethylene glycol) domain were designed, synthesized, and evaluated as a cytophobic surface coating. Such cytophobic, or cell-repellent, coatings are of interest for varied medical and biotech nological applications. The composition of the polystyrene binding peptide domain was identified using an M13 phage display library. ELISA and atomic force spectroscopy were used to evaluate the binding affinity of the amphiphile peptide domain to polystyrene. When coated onto polystyrene, the amphiphile reduced cell adhesion of two distinct mammalian cell lines and pathogenic Staphylococcus aureus strains.
引用
收藏
页码:695 / 700
页数:6
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