Identification of an intracellular domain of the EGF receptor required for high-affinity binding of EGF

被引:20
作者
VanderHeyden, MAG [1 ]
Nievers, M [1 ]
Verkleij, AJ [1 ]
Boonstra, J [1 ]
enHenegouwen, PMPV [1 ]
机构
[1] UNIV UTRECHT,INST BIOMEMBRANES,DEPT MOL CELL BIOL,NL-3584 CH UTRECHT,NETHERLANDS
关键词
EGF; EGF receptor; scatchard analysis; cytoskeleton; F-actin;
D O I
10.1016/S0014-5793(97)00599-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although all EGF receptors in EGF receptor-expressing cells are molecularly identical, they can be subdivided in two different classes that have either a high or a low affinity for EGF, Specifically the high-affinity class is associated with filamentous actin, To determine whether the interaction of the EGF receptor with actin induces its high-affinity state, we studied EGF-binding properties of an EGF receptor mutant that lacks the actin-binding site. Interestingly, we found that cells expressing this mutant receptor still display both high- and low-affinity classes of EGF receptors, indicating that the actin-binding domain does not determine the high-affinity binding state, By further mutational analysis we identified a receptor domain, within the tyrosine kinase domain, that regulates the affinity for EGF. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:265 / 268
页数:4
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