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Ron 受体酪氨酸激酶的跨膜区自身抑制作用。

Autoinhibition of the Ron receptor tyrosine kinase by the juxtamembrane domain.

机构信息

Graduate Program in Cell and Developmental Biology, The Pennsylvania State University, University Park, PA 16802, USA.

出版信息

Cell Commun Signal. 2014 Apr 16;12:28. doi: 10.1186/1478-811X-12-28.

Abstract

BACKGROUND

The Ron receptor tyrosine kinase (RTK) has been implicated in the progression of a number of carcinomas, thus understanding the regulatory mechanisms governing its activity is of potential therapeutic significance. A critical role for the juxtamembrane domain in regulating RTK activity is emerging, however the mechanism by which this regulation occurs varies considerably from receptor to receptor.

RESULTS

Unlike other RTKs described to date, tyrosines in the juxtamembrane domain of Ron are inconsequential for receptor activation. Rather, we have identified an acidic region in the juxtamembrane domain of Ron that plays a central role in promoting receptor autoinhibition. Furthermore, our studies demonstrate that phosphorylation of Y1198 in the kinase domain promotes Ron activation, likely by relieving the inhibitory constraints imposed by the juxtamembrane domain.

CONCLUSIONS

Taken together, our experimental data and molecular modeling provide a better understanding of the mechanisms governing Ron activation, which will lay the groundwork for the development of novel therapeutic approaches for targeting Ron in human malignancies.

摘要

背景

Ron 受体酪氨酸激酶(RTK)已被牵涉到多种癌的进展中,因此,了解调节其活性的调控机制具有潜在的治疗意义。在调节 RTK 活性方面,跨膜区起着关键作用,但这种调节的机制在不同的受体中差异很大。

结果

与迄今为止描述的其他 RTKs 不同,Ron 跨膜区的酪氨酸对于受体激活是无关紧要的。相反,我们已经确定了 Ron 跨膜区中的一个酸性区域,它在促进受体自动抑制中起着核心作用。此外,我们的研究表明,激酶结构域中 Y1198 的磷酸化促进了 Ron 的激活,可能是通过解除跨膜区施加的抑制约束。

结论

总的来说,我们的实验数据和分子建模提供了对 Ron 激活调控机制的更好理解,这将为针对人类恶性肿瘤中 Ron 的新型治疗方法的开发奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/585c/4021555/a16a5570c86f/1478-811X-12-28-1.jpg

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