Chay T R
Department of Biological Sciences, University of Pittsburgh, PA 15260.
J Theor Biol. 1988 Jun 22;132(4):449-68. doi: 10.1016/s0022-5193(88)80084-5.
Allosteric interactions play a crucial role in the regulation of protein-ligand binding. The single-channel recordings of Na+ channels revealed deviations from the Hodgkin-Huxley mechanism, that may be explained in the context of protein co-operativity. In this paper, we present a Na+ channel gating model based on the allosteric nature of the channel proteins. The model contains a co-operative parameter c and a subunit interaction parameter s, in addition to four Hodgkin-Huxley kinetic parameters. Thus, in our model a deviation from the Hodgkin-Huxley mechanism is measured by these two parameters (i.e., whether they are different from unity). We then discuss how to estimate the kinetic parameters in the model from the single channel recordings. Our method of estimating the parameters is tested with Monte Carlo runs with very good results.
变构相互作用在蛋白质-配体结合的调节中起着关键作用。钠通道的单通道记录揭示了与霍奇金-赫胥黎机制的偏差,这可以在蛋白质协同性的背景下得到解释。在本文中,我们提出了一个基于通道蛋白变构性质的钠通道门控模型。该模型除了四个霍奇金-赫胥黎动力学参数外,还包含一个协同参数c和一个亚基相互作用参数s。因此,在我们的模型中,与霍奇金-赫胥黎机制的偏差是由这两个参数来衡量的(即它们是否不同于1)。然后我们讨论了如何从单通道记录中估计模型中的动力学参数。我们估计参数的方法通过蒙特卡洛模拟进行了测试,结果非常好。