Grötzinger Joachim
Department of Biochemistry, Christian-Albrechts-Universität zu Kiel, Germany.
Biochim Biophys Acta. 2002 Nov 11;1592(3):215-23. doi: 10.1016/s0167-4889(02)00316-6.
Cytokine receptors are transmembrane proteins that transmit a signal into the cell upon ligand binding. Commonly, these molecules have one hydrophobic segment of about 20-26 amino acids that is believed to span the membrane as a helix and this divides these receptors into extra- and intracellular components. By utilizing two different epitopes, the cytokines bridge two receptor chains, resulting in a close proximity of the intracellular component and thereby initiating the intracellular signalling cascade. The dimerization event is believed to be the mechanism by which the signal is transmitted across a membrane. In the light of new results obtained for the erythropoietin receptor, James A. Wells questioned whether any dimer would be sufficient. This review will expand upon the above question by discussing the more complex signal-transducing receptor subunits of the Interleukin-6 type family of cytokines. Based on the recently solved quaternary structure of the Insulin receptor, possible analogies will be confronted.
细胞因子受体是跨膜蛋白,在配体结合后将信号传递到细胞内。通常,这些分子有一段约20 - 26个氨基酸的疏水片段,据信该片段以螺旋形式跨膜,这将这些受体分为胞外和胞内组分。通过利用两个不同的表位,细胞因子桥接两条受体链,导致胞内组分紧密靠近,从而启动胞内信号级联反应。二聚化事件被认为是信号跨膜传递的机制。鉴于促红细胞生成素受体获得的新结果,詹姆斯·A·韦尔斯质疑任何二聚体是否都足够。本综述将通过讨论白细胞介素-6型细胞因子家族更复杂的信号转导受体亚基来扩展上述问题。基于最近解析的胰岛素受体四级结构,将探讨可能的类比。