表皮生长因子受体
转录因子
细胞生物学
内吞作用
化学
表皮生长因子
血浆蛋白结合
蛋白质-蛋白质相互作用
受体
生物化学
生物
基因
作者
Lifeng Feng,Xian Wang,Hongchuan Jin,Kaixian Qian,Jian‐Guo Geng
摘要
The binding of Cbl‐interacting protein of 85 kDa (CIN85) to c‐Cbl is important to endocytosis and degradation of epidermal growth factor receptor (EGFR). The proline–arginine motif PXXXPR in c‐Cbl and SH3 domains of CIN85 are essential to this interaction. Here, we demonstrated that SH3KBP1‐binding protein 1 (SHKBP1), which also contains two PXXXPR motifs, constitutively bound to SH3 domains of CIN85. Importantly, the binding of SHKBP1 prevented the interaction of CIN85 with c‐Cbl and inhibited the translocation of CIN85 to EGFR‐containing vesicles, thus reducing EGFR degradation and enhancing EGF‐induced serum response element transcription activity. Therefore, our results indicated that SHKBP1 could promote EGFR signaling pathway by interrupting c‐Cbl‐CIN85 complex and inhibiting EGFR degradation. Copyright © 2011 John Wiley & Sons, Ltd.
科研通智能强力驱动
Strongly Powered by AbleSci AI