Role of the C-terminal linear region of EGF-like growth factors in ErbB specificity

被引:4
|
作者
van der Woning, Sebastian P. [1 ]
Venselaar, Hanka [2 ]
van Rotterdam, Walter [1 ]
Jacobs-Oomen, Saskia [1 ]
van Leeuwen, Jeroen E. M. [1 ]
van Zoelen, Everardus J. J. [1 ]
机构
[1] Radboud Univ Nijmegen, Fac Sci, Dept Cell Biol, NL-6525 AJ Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Ctr Mol & Biomol Informat, NL-6525 GA Nijmegen, Netherlands
关键词
ErbB; homology modelling; binding affinity; mitogenic activity; epidermal growth factor; epiregulin; EXTRACELLULAR DOMAIN; CRYSTAL-STRUCTURE; WILD-TYPE; RECEPTOR; BINDING; AFFINITY; STIMULATION; VARIANTS; BEHAVIOR;
D O I
10.1080/08977190902891010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The epidermal growth factor (EGF)-like growth factors bind their ErbB receptors in a highly selective manner. Recently, we have shown that the sequence YYDLL in the C-terminal linear region is compatible with binding to all ligand-binding ErbB receptors. In the present study, we show that introduction of the YYDLL sequence into the ErbB1 specific ligands EGF and transforming growth factor- (TGF) broadened their receptor specificity towards ErbB4. Upon introduction of the YYDLL sequence into epiregulin, which by itself binds ErbB1 and ErbB4 but not ErbB3, its binding specificity was broadened to ErbB3, concomitant with enhanced affinity for ErbB4. Introduction of the YYDLL sequence into NRG1 resulted in a 10-fold increase in affinity for ErbB3, without affecting its receptor specificity. Remarkably, the strongly enhanced affinity for ErbB3 negatively influenced their mitogenic activity towards cells coexpressing ErbB2 and ErbB3. These observations are discussed in terms of the optimised ErbB affinity, selectivity and mitogenic potential that have taken place during evolution.
引用
收藏
页码:163 / 172
页数:10
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