Reynolds J A, Johnson E A, Tanford C
Proc Natl Acad Sci U S A. 1985 Jun;82(11):3658-61. doi: 10.1073/pnas.82.11.3658.
If a ligand binds with unequal affinity to two distinct states of a protein, then the equilibrium between the two states becomes a function of the concentration of the ligand. A necessary consequence is that the ligand must also affect the forward and/or reverse rate constants for transition between the two states. For an enzyme or transport protein with such a transition as a slow step in the catalytic cycle, the overall rate also becomes a function of ligand concentration. These conclusions are independent of whether or not the ligand is a direct participant in the reaction. If it is a direct participant, then the kinetic effect arising from the principle of linked functions is distinct from the direct catalytic effect. These principles suffice to account for the biphasic response of the hydrolytic activity of ATP-driven ion pumps to the concentration of ATP, without the need to invoke more than one ATP binding site per catalytic center.
如果一种配体以不相等的亲和力与蛋白质的两种不同状态结合,那么这两种状态之间的平衡就成为配体浓度的函数。一个必然的结果是,配体也必须影响两种状态之间转变的正向和/或反向速率常数。对于一种酶或转运蛋白,其转变是催化循环中的慢步骤,那么总体速率也会成为配体浓度的函数。这些结论与配体是否是反应的直接参与者无关。如果它是直接参与者,那么由连锁函数原理产生的动力学效应与直接催化效应是不同的。这些原理足以解释ATP驱动的离子泵水解活性对ATP浓度的双相响应,而无需每个催化中心调用多个ATP结合位点。