Jensen Pia C, Rosenkilde Mette M
Department of Neuroscience and Pharmacology, Laboratory for Molecular Pharmacology, The PanumInstitute, University of Copenhagen, Copenhagen, Denmark.
Methods Enzymol. 2009;461:171-90. doi: 10.1016/S0076-6879(09)05408-1.
Chemokine receptors belong to the large family of 7-transmembrane (7TM) G-protein-coupled receptors. These receptors are targeted and activated by a variety of different ligands, indicating that activation is a result of similar molecular mechanisms but not necessarily similar modes of ligand binding. Attempts to unravel the activation mechanism of 7TM receptors have led to the conclusion that activation involves movements of the transmembrane segments VI and VII in particular, as recently gathered in the Global Toggle Switch Model. However, to understand the activation mechanism completely, more research has to be done in this field. Chemokine receptors are interesting tools in this matter. First, the chemokine system has a high degree of promiscuity that allows several chemokines to target one receptor in different ways, as well as a single chemokine ligand to target several receptors in different ways. Second, the endogenous ligands are large proteins that mainly activate their cognate receptors by interacting with various extracellular-located receptor regions. It is, however, also possible to introduce agonism of simple ligands like metal ions. Thus, the chemokine system offers the possibility to test and compare the activation profiles of several chemically diverse ligands. This also brings up the interesting discussion of allosterism, because small molecules in the chemokine field often interact with allosteric receptor sites.
趋化因子受体属于7次跨膜(7TM)G蛋白偶联受体大家族。这些受体被多种不同的配体靶向并激活,这表明激活是相似分子机制的结果,但配体结合模式不一定相似。试图阐明7TM受体激活机制的研究得出结论,激活尤其涉及跨膜片段VI和VII的移动,这是最近在全球切换开关模型中总结出来的。然而,要完全理解激活机制,该领域还需要开展更多研究。趋化因子受体在此方面是有趣的研究工具。首先,趋化因子系统具有高度的混杂性,这使得几种趋化因子能够以不同方式靶向一种受体,以及单一趋化因子配体能够以不同方式靶向几种受体。其次,内源性配体是大分子蛋白质,它们主要通过与位于细胞外的各种受体区域相互作用来激活其同源受体。然而,引入金属离子等简单配体的激动作用也是可能的。因此,趋化因子系统提供了测试和比较几种化学性质不同的配体激活谱的可能性。这也引发了关于变构的有趣讨论,因为趋化因子领域的小分子常常与变构受体位点相互作用。