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Allostery and cooperativity in the interaction of drugs with ionic channel receptors

机译:药物与离子通道受体相互作用中的变构和协同作用

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摘要

Allostery is an essential property of many physiological mechanisms. Cooperativity together with allostery is observed in the behavior of multisubunit receptors. Here we summarize and compare several approaches to the description and analysis of allosteric phenomena with emphasis on the receptors connected to ionic channels as a model. Several simplified methods are discussed in comparison with the microscopic kinetic scheme. affinity-efficacy separation and a thermodynamic approach.
机译:变构是许多生理机制的基本特性。在多亚基受体的行为中观察到协同作用和变构作用。在这里,我们总结并比较了几种描述和分析变构现象的方法,重点是连接到离子通道的受体作为模型。与微观动力学方案相比,讨论了几种简化方法。亲和力分离和热力学方法。

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