Solution NMR structure of a human FGF-1 monomer, activated by a hexasaccharide heparin-analogue

Authors


J. Jiménez-Barbero, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, 28006 Madrid, Spain
Fax: +34 915360432
Tel: +34 918373112
E-mail: jjbarbero@cib.csic.es

Abstract

The 3D structure of a complex formed by the acidic fibroblast growth factor (FGF-1) and a specifically designed synthetic heparin hexasaccharide has been determined by NMR spectroscopy. This hexasaccharide can substitute natural heparins in FGF-1 mitogenesis assays, in spite of not inducing any apparent dimerization of the growth factor. The use of this well defined synthetic heparin analogue has allowed us to perform a detailed NMR structural analysis of the heparin–FGF interaction, overcoming the limitations of NMR to deal with the high molecular mass and heterogeneity of the FGF-1 oligomers formed in the presence of natural heparin fragments. Our results confirm that glycosaminoglycans induced FGF-1 dimerization either in a cis or trans disposition with respect to the heparin chain is not an absolute requirement for biological activity.

Ancillary