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从 MD 模拟中揭示 PTPN11 SH2 结构域的变构作用。

Revealing Allostery in PTPN11 SH2 Domains from MD Simulations.

机构信息

Theoretical Physics and Center for Biophysics, Saarland University, Saarbrücken, Germany.

出版信息

Methods Mol Biol. 2023;2705:59-75. doi: 10.1007/978-1-0716-3393-9_4.

Abstract

Src-homology 2 (SH2) domains are protein interaction domains that bind to specific peptide motifs containing phosphotyrosine. SHP2, a tyrosine phosphatase encoded by PTPN11 gene, which has been emerged as positive or negative modulator in multiple signaling pathways, contains two SH2 domains, respectively, called N-SH2 and C-SH2. These domains play a relevant role in regulating SHP2 activity, either by recognizing its binding partners or by blocking its catalytic site. Considering the multiple functions that these domains carry out in SHP2, N-SH2 and C-SH2 represent an interesting case of study. In this chapter, we present a methodology that permits, by means of the principal component analysis (PCA), to study and to rationalize the structures adopted by the SH2 domains, in terms of the conformations of their binding sites. The structures can be distinguished, grouped, classified, and reported in a diagram. This approach permits to identify the accessible conformations of the SH2 domains in different binding conditions and to eventually reveal allosteric interactions. The method further reveals that the conformation dynamics of N-SH2 and C-SH2 strongly differ, which likely reflects their distinct functional roles.

摘要

Src 同源结构域 2(SH2)是一种蛋白相互作用结构域,能够与含有磷酸酪氨酸的特定肽基序结合。SHP2 是由 PTPN11 基因编码的一种酪氨酸磷酸酶,它在多种信号通路中作为正或负调节剂发挥作用,包含两个 SH2 结构域,分别称为 N-SH2 和 C-SH2。这些结构域在调节 SHP2 活性方面发挥着重要作用,或者通过识别其结合伙伴,或者通过阻止其催化位点。考虑到这些结构域在 SHP2 中执行的多种功能,N-SH2 和 C-SH2 代表了一个有趣的研究案例。在本章中,我们提出了一种方法,通过主成分分析(PCA),可以研究和合理化 SH2 结构域的结构,从其结合位点的构象方面进行研究。这些结构可以被区分、分组、分类,并在图表中报告。这种方法可以识别不同结合条件下 SH2 结构域的可及构象,并最终揭示变构相互作用。该方法进一步表明,N-SH2 和 C-SH2 的构象动力学差异很大,这可能反映了它们不同的功能作用。

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