West David C, Rees Chris G, Duchesne Laurence, Patey Susannah J, Terry Carla J, Turnbull Jeremy E, Delehedde Maryse, Heegaard Christian W, Allain Fabrice, Vanpouille Christophe, Ron Dina, Fernig David G
School of Biological Sciences, Biosciences Building, University of Liverpool, Liverpool, L69 7ZB, United Kingdom.
J Biol Chem. 2005 Apr 8;280(14):13457-64. doi: 10.1074/jbc.M410924200. Epub 2005 Feb 4.
The hypothesis that neuropilin-1 (Npn-1) may interact with heparin-binding proteins other than vascular endothelial growth factor has been tested using an optical biosensor-based binding assay. The results show that fibroblast growth factor (FGF) 1, 2, 4, and 7, FGF receptor 1, hepatocyte growth factor/scatter factor (HGF/SF), FGF-binding protein, normal protease sensitive form of prion protein, antithrombin III, and Npn-1 itself are all able to interact with Npn-1 immobilized on the sensor surface. FGF-2, FGF-4, and HGF/SF are also shown to interact with Npn-1 in a solution assay. Moreover, these protein-protein interactions are dependent on the ionic strength of the medium and are inhibited by heparin, and the kinetics of binding of FGF-2, FGF-4 and HGF/SF to Npn-1 are characterized by fast association rate constants (270,000-1,600,000 m(-1) s(-1)). These results suggest that Npn-1 possesses a "heparin" mimetic site that is able to interact at least in part through ionic bonding with the heparin binding site on many of the proteins studied. Npn-1 was also found to potentiate the growth stimulatory activity of FGF-2 on human umbilical vein endothelial cells, indicating that Npn-1 may not just bind but also regulate the activity of heparin-binding proteins.
已使用基于光学生物传感器的结合试验对神经纤毛蛋白-1(Npn-1)可能与血管内皮生长因子以外的肝素结合蛋白相互作用这一假说进行了验证。结果表明,成纤维细胞生长因子(FGF)1、2、4和7、FGF受体1、肝细胞生长因子/扩散因子(HGF/SF)、FGF结合蛋白、正常蛋白酶敏感形式的朊病毒蛋白、抗凝血酶III以及Npn-1自身均能够与固定在传感器表面的Npn-1相互作用。在溶液试验中还表明,FGF-2、FGF-4和HGF/SF也能与Npn-1相互作用。此外,这些蛋白质-蛋白质相互作用依赖于介质的离子强度,并受到肝素的抑制,FGF-2、FGF-4和HGF/SF与Npn-1结合的动力学特征是具有快速缔合速率常数(270,000 - 1,600,000 m(-1)s(-1))。这些结果表明,Npn-1具有一个“肝素”模拟位点,该位点能够至少部分地通过离子键与许多所研究蛋白质上的肝素结合位点相互作用。还发现Npn-1可增强FGF-2对人脐静脉内皮细胞的生长刺激活性,这表明Npn-1可能不仅能结合肝素结合蛋白,还能调节其活性。