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促甲状腺激素受体上的跨膜吸引域。

Transmembrane domains of attraction on the TSH receptor.

机构信息

Thyroid Research Unit (R.L., M.R.A., T.F.D.) and Departments of Medicine (R.L., M.R.A., T.F.D.) and Structural and Chemical Biology (M.M.), Icahn School of Medicine at Mt Sinai School of Medicine, New York, New York 10029; and James J. Peters Veterans Affairs Medical Center (R.L., M.R.A., T.F.D.), New York, New York 10468.

出版信息

Endocrinology. 2015 Feb;156(2):488-98. doi: 10.1210/en.2014-1509. Epub 2014 Nov 19.

Abstract

The TSH receptor (TSHR) has the propensity to form dimers and oligomers. Our data using ectodomain-truncated TSHRs indicated that the predominant interfaces for oligomerization reside in the transmembrane (TM) domain. To map the potentially interacting residues, we first performed in silico studies of the TSHR transmembrane domain using a homology model and using Brownian dynamics (BD). The cluster of dimer conformations obtained from BD analysis indicated that TM1 made contact with TM4 and two residues in TM2 made contact with TM5. To confirm the proximity of these contact residues, we then generated cysteine mutants at all six contact residues predicted by the BD analysis and performed cysteine cross-linking studies. These results showed that the predicted helices in the protomer were indeed involved in proximity interactions. Furthermore, an alternative experimental approach, receptor truncation experiments and LH receptor sequence substitution experiments, identified TM1 harboring a major region involved in TSHR oligomerization, in agreement with the conclusion from the cross-linking studies. Point mutations of the predicted interacting residues did not yield a substantial decrease in oligomerization, unlike the truncation of the TM1, so we concluded that constitutive oligomerization must involve interfaces forming domains of attraction in a cooperative manner that is not dominated by interactions between specific residues.

摘要

促甲状腺激素受体(TSHR)有形成二聚体和寡聚体的倾向。我们使用截短胞外结构域的 TSHR 的数据表明,寡聚化的主要界面位于跨膜(TM)域。为了绘制潜在的相互作用残基,我们首先使用同源模型和布朗动力学(BD)对 TSHR 跨膜域进行了计算机模拟研究。BD 分析获得的二聚体构象簇表明 TM1 与 TM4 接触,TM2 中的两个残基与 TM5 接触。为了确认这些接触残基的接近程度,我们随后在 BD 分析预测的所有六个接触残基处生成了半胱氨酸突变体,并进行了半胱氨酸交联研究。这些结果表明,原聚体中预测的螺旋确实参与了接近相互作用。此外,受体截断实验和 LH 受体序列取代实验等替代实验方法确定 TM1 含有参与 TSHR 寡聚化的主要区域,与交联研究的结论一致。与 TM1 的截断不同,预测相互作用残基的点突变并未导致寡聚化的显著降低,因此我们得出结论,组成型寡聚化必须涉及以协同方式形成吸引力域的界面,而不是由特定残基之间的相互作用主导。

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