van der Woning Sebastian P, Venselaar Hanka, van Rotterdam Walter, Jacobs-Oomen Saskia, van Leeuwen Jeroen E M, van Zoelen Everardus J J
Department of Cell Biology, Faculty of Science, Radboud University Nijmegen, Nijmegen, The Netherlands.
Growth Factors. 2009 Jun;27(3):163-72. doi: 10.1080/08977190902891010.
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-alpha (TGFalpha) 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 NRG1beta 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.
表皮生长因子(EGF)样生长因子以高度选择性的方式结合其ErbB受体。最近,我们已经表明,C末端线性区域中的YYDLL序列与结合所有配体结合型ErbB受体兼容。在本研究中,我们表明,将YYDLL序列引入ErbB1特异性配体EGF和转化生长因子-α(TGFα)中,拓宽了它们对ErbB4的受体特异性。将YYDLL序列引入上皮调节蛋白(其自身结合ErbB1和ErbB4,但不结合ErbB3)后,其结合特异性拓宽至ErbB3,同时对ErbB4的亲和力增强。将YYDLL序列引入NRG1β导致对ErbB3的亲和力增加10倍,而不影响其受体特异性。值得注意的是,对ErbB3的强烈增强亲和力对它们对共表达ErbB2和ErbB3的细胞的促有丝分裂活性产生了负面影响。根据进化过程中发生的优化的ErbB亲和力、选择性和促有丝分裂潜力对这些观察结果进行了讨论。