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TEAD4-YAP/TAZ 蛋白-蛋白相互作用:预期的相似性和意想不到的差异。

The TEAD4-YAP/TAZ protein-protein interaction: expected similarities and unexpected differences.

机构信息

Disease Area Oncology, Novartis Institutes for Biomedical Research, 141 Klybeckstrasse, 4057 Basel, Switzerland.

出版信息

Chembiochem. 2013 Jul 8;14(10):1218-25. doi: 10.1002/cbic.201300163. Epub 2013 Jun 18.

Abstract

The Hippo pathway controls cell homeostasis, and its deregulation can lead to human diseases. In this pathway, the YAP and TAZ transcriptional cofactors play a key role in stimulating gene transcription through their interaction with the TEAD transcriptional factors. Our study of YAP and TAZ peptides in biochemical and biophysical assays shows that both proteins have essentially the same affinity for TEAD. Molecular modeling and structural biology data suggest that they also bind to the same site on TEAD. However, this apparent similarity hides differences in the ways in which the two proteins interact with TEAD. The secondary structure elements of their TEAD binding site do not contribute equally to the overall affinity, and critical interactions with TEAD are made through different residues. This convergent optimization of the YAP/TAZ TEAD binding site suggests that the similarity in the affinities of binding of YAP to TEAD and of TAZ to TEAD is important for Hippo pathway functionality.

摘要

Hippo 通路控制细胞内稳态,其失调可导致人类疾病。在该通路中,YAP 和 TAZ 转录共激活因子通过与 TEAD 转录因子相互作用,在刺激基因转录方面发挥关键作用。我们在生化和生物物理测定中对 YAP 和 TAZ 肽的研究表明,这两种蛋白质对 TEAD 的亲和力基本相同。分子建模和结构生物学数据表明,它们也结合到 TEAD 的相同位点。然而,这种明显的相似性掩盖了两种蛋白质与 TEAD 相互作用方式的差异。它们的 TEAD 结合位点的二级结构元件对整体亲和力的贡献并不相同,并且与 TEAD 的关键相互作用是通过不同的残基形成的。YAP/TAZ TEAD 结合位点的这种趋同优化表明,YAP 与 TEAD 的结合亲和力和 TAZ 与 TEAD 的结合亲和力的相似性对 Hippo 通路的功能很重要。

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