
doi: 10.1021/bc034138t
pmid: 14733594
Mono- and disaccharide-containing glycopolymers were synthesized by cyanoxyl-mediated polymerization of acrylamide with acrylate-derivatized mono- and disaccharides. We demonstrate that a glycopolymer bearing pendant, fully sulfated lactose units effectively replaces heparin and heparan sulfate as a molecular chaperone for fibroblast growth factor-2 (FGF-2). Specifically, a compound was identified that protects FGF-2 from proteolytic, acid, and heat-induced degradation, while selectively promoting growth factor and receptor dimerization. Significantly, the capacity of this heparin-mimic to promote an FGF-2 specific proliferative cell response was confirmed and suggests potential applications for this compound and related derivatives in areas related to therapeutic angiogenesis.
Hot Temperature, Polymers, Hydrolysis, Molecular Mimicry, Receptor Protein-Tyrosine Kinases, Receptors, Fibroblast Growth Factor, Mice, Solvents, Animals, Fibroblast Growth Factor 2, Indicators and Reagents, Trypsin, Chromatography, Thin Layer, Receptor, Fibroblast Growth Factor, Type 1, Acids, Cell Division, Cells, Cultured, Molecular Chaperones
Hot Temperature, Polymers, Hydrolysis, Molecular Mimicry, Receptor Protein-Tyrosine Kinases, Receptors, Fibroblast Growth Factor, Mice, Solvents, Animals, Fibroblast Growth Factor 2, Indicators and Reagents, Trypsin, Chromatography, Thin Layer, Receptor, Fibroblast Growth Factor, Type 1, Acids, Cell Division, Cells, Cultured, Molecular Chaperones
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