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BMP 受体的结构见解:特异性、激活和抑制。

Structural insights into BMP receptors: Specificity, activation and inhibition.

机构信息

Institute for Chemistry and Biochemistry, Free University Berlin, Institute of Chemistry and Biochemistry, D-14195 Berlin, Germany; Berlin-Brandenburg School for Regenerative Therapies (BSRT), Charité Campus Virchow Klinikum, Augustenburger Platz 1, D-13351 Berlin, Germany.

Molecular Plant Physiology and Biophysics, Julius-von-Sachs-Institute of the University Wuerzburg, Julius-von-Sachs-Platz 2, D-97082 Wuerzburg, Germany.

出版信息

Cytokine Growth Factor Rev. 2016 Feb;27:13-34. doi: 10.1016/j.cytogfr.2015.11.005. Epub 2015 Nov 24.

Abstract

Bone morphogenetic proteins (BMPs) are members of the transforming growth factor-β family (TGFβ), which signal through hetero-tetrameric complexes of type I and type II receptors. In humans there are many more TGFβ ligands than receptors, leading to the question of how particular ligands can initiate specific signaling responses. Here we review structural features of the ligands and receptors that contribute to this specificity. Ligand activity is determined by receptor-ligand interactions, growth factor prodomains, extracellular modulator proteins, receptor assembly and phosphorylation of intracellular signaling proteins, including Smad transcription factors. Detailed knowledge about the receptors has enabled the development of BMP-specific type I receptor kinase inhibitors. In future these may help to treat human diseases such as fibrodysplasia ossificans progressiva.

摘要

骨形态发生蛋白(BMPs)是转化生长因子-β家族(TGFβ)的成员,通过 I 型和 II 型受体的异型三聚体复合物传递信号。在人类中,TGFβ 配体的数量远远超过受体,这就提出了一个问题,即特定的配体如何引发特定的信号响应。在这里,我们综述了配体和受体的结构特征,这些特征有助于配体的特异性。配体活性由受体-配体相互作用、生长因子前导序列、细胞外调节剂蛋白、受体组装以及包括 Smad 转录因子在内的细胞内信号蛋白的磷酸化决定。对受体的详细了解使 BMP 特异性 I 型受体激酶抑制剂的开发成为可能。将来,这些抑制剂可能有助于治疗纤维发育不良性骨化性肌炎等人类疾病。

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