Bouhaddou Mehdi, Birtwistle Marc R
Icahn School of Medicine at Mount Sinai, Department of Pharmacology and Systems Therapeutics, New York, NY 10029, USA.
Mol Biosyst. 2014 Jul;10(7):1824-32. doi: 10.1039/c4mb00022f.
Cooperativity of ligand-receptor binding influences the input-output behavior of a biochemical system and thus is an important determinant of its physiological function. Canonically, such cooperativity is understood in terms of ligand-receptor binding affinity, where an initial binding event changes the affinity for subsequent binding events. Here, we demonstrate that dimerization-a simple yet pervasive signaling motif across biology-can have significant control over cooperativity and even dominate over the canonical mechanism. Through an exhaustive parameter sensitivity analysis of a general kinetic model for signal-mediated dimerization, we show that quantitative modulation of dimerization processes can reinforce, eliminate, and even reverse cooperativity imposed by the canonical allosteric ligand-receptor binding affinity mechanism. The favored accumulation of stoichiometrically asymmetric dimers (those with ligand-receptor stoichiometry of 1 : 2) is a major determinant of dimerization-based cooperativity control. However, simulations demonstrate that favoring accumulation of such stoichiometrically asymmetric dimers can either increase or decrease cooperativity, and thus the quantitative relationship between stoichiometrically asymmetric dimers and cooperativity is highly dependent on the parameter values of the particular system of interest. These results suggest that the dimerization motif provides a novel mechanism for both generating and quantitatively tuning cooperativity that, due to the ubiquity of dimerization motifs in biochemical systems, may play a major role in a host of biological functions. Thus, the canonical, allosteric view of cooperativity is incomplete without considering dimerization effects, which is of particular importance as dimerization is often a necessary feature of the allosteric mechanism.
配体-受体结合的协同性会影响生化系统的输入-输出行为,因此是其生理功能的一个重要决定因素。传统上,这种协同性是根据配体-受体结合亲和力来理解的,即初始结合事件会改变对后续结合事件的亲和力。在此,我们证明二聚化——一种在生物学中简单却普遍存在的信号基序——能够对协同性进行显著控制,甚至能主导传统机制。通过对信号介导二聚化的通用动力学模型进行详尽的参数敏感性分析,我们表明二聚化过程的定量调节可以增强、消除甚至逆转由传统变构配体-受体结合亲和力机制施加的协同性。化学计量不对称二聚体(那些配体-受体化学计量为1:2的二聚体)的优先积累是基于二聚化的协同性控制的一个主要决定因素。然而,模拟结果表明,促进这种化学计量不对称二聚体的积累既可以增加也可以降低协同性,因此化学计量不对称二聚体与协同性之间的定量关系高度依赖于特定感兴趣系统的参数值。这些结果表明,二聚化基序为产生和定量调节协同性提供了一种新机制,由于二聚化基序在生化系统中普遍存在,它可能在许多生物学功能中发挥主要作用。因此,如果不考虑二聚化效应,传统的协同性变构观点是不完整的,这一点尤为重要,因为二聚化往往是变构机制的一个必要特征。