TY - JOUR A1 - Volz, Yvonne A1 - Koschut, David A1 - Matzke-Og, Alexandra A1 - Dietz, Marina A1 - Karathanasis, Christos A1 - Richert, Ludovic A1 - Wagner, Moritz G. A1 - Mély, Yves A1 - Heilemann, Mike A1 - Niemann, Hartmut H. A1 - Orian-Rousseau, Véronique T1 - Direct binding of hepatocyte growth factor and vascular endothelial growth factor to CD44v6 T2 - Bioscience reports N2 - CD44v6, a member of the CD44 family of transmembrane glycoproteins is a co-receptor for two receptor tyrosine kinases (RTKs), Met and VEGFR-2 (vascular endothelial growth factor receptor 2). CD44v6 is not only required for the activation of these RTKs but also for signalling. In order to understand the role of CD44v6 in Met and VEGFR-2 activation and signalling we tested whether CD44v6 binds to their ligands, HGF (hepatocyte growth factor) and VEGF (vascular endothelial growth factor), respectively. FACS analysis and cellular ELISA showed binding of HGF and VEGF only to cells expressing CD44v6. Direct binding of CD44v6 to HGF and VEGF was demonstrated in pull-down assays and the binding affinities were determined using MicroScale Thermophoresis, fluorescence correlation spectroscopy and fluorescence anisotropy. The binding affinity of CD44v6 to HGF is in the micromolar range in contrast with the high-affinity binding measured in the case of VEGF and CD44v6, which is in the nanomolar range. These data reveal a heparan sulfate-independent direct binding of CD44v6 to the ligands of Met and VEGFR-2 and suggest different roles of CD44v6 for these RTKs. KW - binding affinity KW - CD44s KW - CD44v6 KW - HGF KW - Met KW - VEGF Y1 - 2015 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/44545 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-445453 SN - 1573-4935 SN - 0144-8463 N1 - © 2015 Authors This is an open access article published by Portland Press Limited and distributed under the Creative Commons Attribution Licence 3.0 VL - 35 IS - 4, e00236 SP - 1 EP - 16 PB - Portland Press CY - Colchester ER -