Schaarschmidt Joerg, Nagel Marcus B M, Huth Sandra, Jaeschke Holger, Moretti Rocco, Hintze Vera, von Bergen Martin, Kalkhof Stefan, Meiler Jens, Paschke Ralf
Department of Internal Medicine, University of Leipzig, 04103 Leipzig, Germany.
Department of Internal Medicine, University of Leipzig, 04103 Leipzig, Germany,; Department of Proteomics, Helmholtz-Centre for Environmental Research, 04318 Leipzig, Germany.
J Biol Chem. 2016 Jul 1;291(27):14095-14108. doi: 10.1074/jbc.M115.709659. Epub 2016 Apr 26.
The thyroid stimulating hormone receptor (TSHR) is a G protein-coupled receptor (GPCR) with a characteristic large extracellular domain (ECD). TSHR activation is initiated by binding of the hormone ligand TSH to the ECD. How the extracellular binding event triggers the conformational changes in the transmembrane domain (TMD) necessary for intracellular G protein activation is poorly understood. To gain insight in this process, the knowledge on the relative positioning of ECD and TMD and the conformation of the linker region at the interface of ECD and TMD are of particular importance. To generate a structural model for the TSHR we applied an integrated structural biology approach combining computational techniques with experimental data. Chemical cross-linking followed by mass spectrometry yielded 17 unique distance restraints within the ECD of the TSHR, its ligand TSH, and the hormone-receptor complex. These structural restraints generally confirm the expected binding mode of TSH to the ECD as well as the general fold of the domains and were used to guide homology modeling of the ECD. Functional characterization of TSHR mutants confirms the previously suggested close proximity of Ser-281 and Ile-486 within the TSHR. Rigidifying this contact permanently with a disulfide bridge disrupts ligand-induced receptor activation and indicates that rearrangement of the ECD/extracellular loop 1 (ECL1) interface is a critical step in receptor activation. The experimentally verified contact of Ser-281 (ECD) and Ile-486 (TMD) was subsequently utilized in docking homology models of the ECD and the TMD to create a full-length model of a glycoprotein hormone receptor.
促甲状腺激素受体(TSHR)是一种G蛋白偶联受体(GPCR),具有特征性的大细胞外结构域(ECD)。TSHR的激活是由激素配体促甲状腺激素(TSH)与ECD结合引发的。细胞外结合事件如何触发细胞内G蛋白激活所需的跨膜结构域(TMD)的构象变化,目前尚不清楚。为了深入了解这一过程,了解ECD和TMD的相对定位以及ECD和TMD界面处连接区的构象尤为重要。为了生成TSHR的结构模型,我们应用了一种综合结构生物学方法,将计算技术与实验数据相结合。化学交联后进行质谱分析,在TSHR的ECD、其配体TSH以及激素-受体复合物中产生了17个独特的距离限制。这些结构限制通常证实了TSH与ECD的预期结合模式以及各结构域的总体折叠,并用于指导ECD的同源建模。TSHR突变体的功能表征证实了之前提出的TSHR内Ser-281和Ile-486的紧密接近。用二硫键永久固定这种接触会破坏配体诱导的受体激活,并表明ECD/细胞外环1(ECL1)界面的重排是受体激活的关键步骤。随后,利用实验验证的Ser-281(ECD)和Ile-486(TMD)的接触,对接ECD和TMD的同源模型,以创建糖蛋白激素受体的全长模型。