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G蛋白偶联受体激活的建模:无药物组成型受体活性

Modelling of the activation of G-protein coupled receptors: drug free constitutive receptor activity.

作者信息

Woodroffe P J, Bridge L J, King J R, Chen C Y, Hill S J

机构信息

Centre for Mathematical Medicine, Division of Theoretical Mechanics, School of Mathematical Sciences, University of Nottingham, Nottingham, UK.

出版信息

J Math Biol. 2010 Mar;60(3):313-46. doi: 10.1007/s00285-009-0268-5. Epub 2009 Apr 5.

Abstract

G-protein coupled receptors (GPCRs) form a crucial component of approximately 80% of hormone pathways. In this paper, the most popular mechanism for activation of GPCRs-the shuttling mechanism-is modelled mathematically. An asymptotic analysis of this model clarifies the dynamics of the system in the absence of drug, in particular which reactions dominate during the different timescales. Equilibrium analysis of the model demonstrates the model's ability to predict constitutive receptor activity.

摘要

G蛋白偶联受体(GPCRs)构成了约80%的激素信号通路的关键组成部分。在本文中,对GPCRs激活的最常见机制——穿梭机制进行了数学建模。对该模型的渐近分析阐明了无药物情况下系统的动力学,特别是在不同时间尺度上哪些反应起主导作用。该模型的平衡分析证明了其预测组成型受体活性的能力。

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