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Modeling Signal Transduction Involving G Protein Coupled Receptors by Genetic Algorithm and Nonlinear Spatiotemporal Analysis

机译:遗传算法和非线性时空分析涉及G蛋白偶联受体的模拟信号转导

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In this paper, modeling of the signal transduction process involving G proteins is done with the utilization of genetic algorithm and a weakly nonlinear analysis. Equations which govern the interaction between an inhibitor protein and the ligand-receptor complexes are written and fitted with experimental data of cAMP levels expressed at different elapsed times, in the case that the homogeneous distribution of ligand-receptor complexes is assumed over the surface membrane. The model is then modified to incorporate reaction-diffusion mechanisms whereby the ligand-receptor complexes and the inhibiting agents in the process may diffuse over the cell membrane. We investigate the formation of Turing-type patterns under certain conditions on the system parameters which characterize the formation of stationary symmetry breaking structures; stripes and hexagonal arrays of spots or nets over the cell membrane.
机译:本文利用遗传算法和弱非线性分析,采用涉及G蛋白的信号转导过程的建模。在不同经过时间在不同经过时间表示的CAMP水平的实验数据写入并配合治理抑制剂蛋白和配体 - 受体复合物之间的相互作用的等式,在所述配体 - 受体络合物的均匀分布在表面膜上。然后修饰该模型以掺入反应扩散机制,由此可以在细胞膜中扩散配体 - 受体复合物和该方法中的抑制剂。我们在系统参数的某些条件下调查图灵型模式的形成,其表征了静止对称破碎结构的形成;细胞膜上的条纹和六角形或网阵列。

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