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Harmonic oscillator model of the insulin and IGF1 receptors allosteric binding and activation

机译:胰岛素和IGF1受体的变构结合与​​激活的谐波振荡器模型

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摘要

The insulin and insulin-like growth factor 1 receptors activate overlapping signalling pathways that are critical for growth, metabolism, survival and longevity. Their mechanism of ligand binding and activation displays complex allosteric properties, which no mathematical model has been able to account for. Modelling these receptors' binding and activation in terms of interactions between the molecular components is problematical due to many unknown biochemical and structural details. Moreover, substantial combinatorial complexity originating from multivalent ligand binding further complicates the problem. On the basis of the available structural and biochemical information, we develop a physically plausible model of the receptor binding and activation, which is based on the concept of a harmonic oscillator. Modelling a network of interactions among all possible receptor intermediaries arising in the context of the model (35, for the insulin receptor) accurately reproduces for the first time all the kinetic properties of the receptor, and provides unique and robust estimates of the kinetic parameters. The harmonic oscillator model may be adaptable for many other dimeric/dimerizing receptor tyrosine kinases, cytokine receptors and G-protein-coupled receptors where ligand crosslinking occurs.
机译:胰岛素和类胰岛素生长因子1受体激活重叠的信号通路,这对于生长,代谢,存活和寿命至关重要。它们的配体结合和激活机制显示出复杂的变构特性,这是任何数学模型都无法解释的。由于许多未知的生化和结构细节,根据分子组分之间的相互作用对这些受体的结合和激活进行建模是有问题的。而且,源自多价配体结合的大量组合复杂性进一步使该问题复杂化。根据可用的结构和生化信息,我们开发了一种基于谐波振荡器概念的受体结合和激活的物理模型。在模型的背景下(对于胰岛素受体为35),对所有可能的受体中间物之间的相互作用网络进行建模,将首次准确地再现受体的所有动力学特性,并提供动力学参数的唯一且可靠的估计。谐波振荡器模型可能适用于发生配体交联的许多其他二聚/二聚受体酪氨酸激酶,细胞因子受体和G蛋白偶联受体。

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