Suppr超能文献

表皮生长因子受体的自身磷酸化:分子间变构激活模型的证据

Self-phosphorylation of epidermal growth factor receptor: evidence for a model of intermolecular allosteric activation.

作者信息

Yarden Y, Schlessinger J

出版信息

Biochemistry. 1987 Mar 10;26(5):1434-42. doi: 10.1021/bi00379a034.

Abstract

The membrane receptor for epidermal growth factor (EGF) is a 170,000-dalton glycoprotein composed of an extracellular EGF-binding domain and a cytoplasmic kinase domain connected by a stretch of 23 amino acids traversing the plasma membrane. The binding of EGF to the extracellular domain activates the cytoplasmic kinase function even in highly purified preparations of EGF receptor, suggesting that the activation occurs exclusively within the EGF receptor moiety. Conceivably, kinase activation may require the transfer of a conformational change through the single transmembrane region from the ligand binding domain to the cytoplasmic kinase region. Alternatively, ligand-induced receptor-receptor interactions may activate the kinase and thus bypass this requirement. Both mechanisms were contrasted by employing independent experimental approaches. The following lines of evidence support an intermolecular mechanism for the activation of the detergent-solubilized receptor: the EGF-induced receptor self-phosphorylation has a parabolic dependence on the concentration of EGF receptor, cross-linking of EGF receptors by antibodies or lectins stimulates receptor self-phosphorylation, immobilization of EGF receptor on various solid matrices prevents EGF from activating the kinase function, and cross-linking of EGF receptors increases their affinity toward EGF. On the basis of these results, an allosteric aggregation model is formulated for the activation of the cytoplasmic kinase function of the receptor by EGF. This model may be relevant to the mechanism by which the mitogenic signal of EGF is transferred across the membrane.

摘要

表皮生长因子(EGF)的膜受体是一种170,000道尔顿的糖蛋白,由一个细胞外EGF结合结构域和一个细胞质激酶结构域组成,二者通过一段穿越质膜的23个氨基酸相连。即使在高度纯化的EGF受体制剂中,EGF与细胞外结构域的结合也会激活细胞质激酶功能,这表明激活仅在EGF受体部分内发生。可以想象,激酶激活可能需要通过单个跨膜区域将构象变化从配体结合结构域传递到细胞质激酶区域。或者,配体诱导的受体-受体相互作用可能激活激酶,从而绕过这一要求。通过采用独立的实验方法对这两种机制进行了对比。以下一系列证据支持去污剂溶解受体激活的分子间机制:EGF诱导的受体自磷酸化对EGF受体浓度呈抛物线依赖性,抗体或凝集素对EGF受体的交联刺激受体自磷酸化,EGF受体固定在各种固体基质上会阻止EGF激活激酶功能,EGF受体的交联增加了它们对EGF的亲和力。基于这些结果,提出了一个变构聚集模型,用于EGF激活受体的细胞质激酶功能。该模型可能与EGF的促有丝分裂信号跨膜传递的机制有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验