Valero Edelmira, García-Moreno Manuela, Masiá Jesualdo, García-Meseguer María-José, Varón Ramón
Departamento de Química-Física. Escuela Politécnica Superior de Albacete. Universidad de Castilla-La Mancha. Campus Universitario. E-02071-Albacete, Spain.
J Theor Biol. 2007 Mar 7;245(1):175-92. doi: 10.1016/j.jtbi.2006.09.020. Epub 2006 Sep 24.
In the present paper, a kinetic analysis of a general model for proenzyme activation, where the activating enzyme and also the activated one are reversibly inhibited in two steps by two different inhibitors, has been performed. The cases in which both inhibitors are the same, or in which the inhibition is irreversible (only one or the two inhibition routes) are treated as particular cases of the general model. In addition, the kinetic behaviour of many other proenzyme activation systems involving inhibition, particular cases of the reaction scheme under study, can be obtained. The total number of particular cases for the general model under study is 370, so this approach offers to the scientific community working in limited proteolysis regulation for the first time a method based on general solutions which only needs to be specified to their concrete problem of zymogen activation. Finally, new adimensional parameters are introduced, allowing the knowledgement, in the case that any of the inhibition routes is irreversible, the relative weight of both activation and irreversible inhibition routes.
在本文中,对一种酶原激活通用模型进行了动力学分析,其中激活酶以及被激活的酶在两个步骤中被两种不同的抑制剂可逆抑制。两种抑制剂相同的情况,或者抑制是不可逆的情况(仅一条或两条抑制途径)被视为通用模型的特殊情况。此外,还可以得到许多其他涉及抑制的酶原激活系统的动力学行为,这些都是所研究反应方案的特殊情况。所研究的通用模型的特殊情况总数为370种,因此这种方法首次为从事有限蛋白水解调节研究的科学界提供了一种基于通用解的方法,该方法只需针对其具体的酶原激活问题进行具体化。最后,引入了新的无量纲参数,在任何一条抑制途径不可逆的情况下,能够了解激活途径和不可逆抑制途径的相对权重。