Fibroblast growth factors (FGFs) require a polysaccharide cofactor, heparin or heparan sulfate (HS), for receptor binding and activation. To probe the molecular mechanism by which heparin or HS (heparin/HS) activates FGF, small nonsulfated oligosaccharides found within heparin/HS were assayed for activity. These synthetic and isomerically pure compounds can activate the FGF signaling pathway. The crystal structures of complexes between FGF and these heparin/HS oligosaccharides reveal several binding sites on FGF and constrain possible mechanisms by which heparin/HS can activate the FGF receptor. These studies establish a framework for the molecular design of compounds capable of modulating FGF activity
Fibroblast growth factors (FGFs) are a large family of structurally related proteins with a wide ran...
Interaction of basic fibroblast growth factor (bFGF) with heparan sulfate proteoglycans (HSPGs) play...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2002.Includ...
Heparan sulfate (HS) belongs to the glycosaminoglycan family of polysaccharides and is found attache...
Heparan sulfate (HS) belongs to the glycosaminoglycan family of polysaccharides and is found attache...
AbstractSignalling by fibroblast growth factors (FGFs) through FGF receptors (FGFRs) depends on the ...
AbstractFibroblast growth factors and their receptors bind to heparan sulfate glycosaminoglycans. Th...
The interaction of heparan sulfate (HS) (and the closely related molecule heparin) with FGF-1 is a r...
The role of heparin or heparan sulfates in the interaction of basic fibroblast growth factor (bFGF) ...
AbstractFibroblast growth factors and their receptors bind to heparan sulfate glycosaminoglycans. Th...
ABSTRACT: Heparan sulfate (HS) proteoglycans (PGs) interact with a number of extracellular signaling...
Heparan sulfate proteoglycans (HSPG) are obligatory for receptor binding and mitogenic activity of b...
Fibroblast growth factors (FGFs) are members of a protein family with a broad range of biological ac...
Fibroblast growth factors (FGFs) are members of a protein family with a broad range of biological ac...
The glycosaminoglyeans heparin and heparan sulfate (HS) bind to fibroblast growth factor FGF1 and pr...
Fibroblast growth factors (FGFs) are a large family of structurally related proteins with a wide ran...
Interaction of basic fibroblast growth factor (bFGF) with heparan sulfate proteoglycans (HSPGs) play...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2002.Includ...
Heparan sulfate (HS) belongs to the glycosaminoglycan family of polysaccharides and is found attache...
Heparan sulfate (HS) belongs to the glycosaminoglycan family of polysaccharides and is found attache...
AbstractSignalling by fibroblast growth factors (FGFs) through FGF receptors (FGFRs) depends on the ...
AbstractFibroblast growth factors and their receptors bind to heparan sulfate glycosaminoglycans. Th...
The interaction of heparan sulfate (HS) (and the closely related molecule heparin) with FGF-1 is a r...
The role of heparin or heparan sulfates in the interaction of basic fibroblast growth factor (bFGF) ...
AbstractFibroblast growth factors and their receptors bind to heparan sulfate glycosaminoglycans. Th...
ABSTRACT: Heparan sulfate (HS) proteoglycans (PGs) interact with a number of extracellular signaling...
Heparan sulfate proteoglycans (HSPG) are obligatory for receptor binding and mitogenic activity of b...
Fibroblast growth factors (FGFs) are members of a protein family with a broad range of biological ac...
Fibroblast growth factors (FGFs) are members of a protein family with a broad range of biological ac...
The glycosaminoglyeans heparin and heparan sulfate (HS) bind to fibroblast growth factor FGF1 and pr...
Fibroblast growth factors (FGFs) are a large family of structurally related proteins with a wide ran...
Interaction of basic fibroblast growth factor (bFGF) with heparan sulfate proteoglycans (HSPGs) play...
Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2002.Includ...