Weingand-Ziade A, Ribes F, Renault F, Masson P
Centre de Recherches du Service de Santé des Armées, Unité d'Enzymologie, BP 87, 38702 La Tronche Cédex, France.
Biochem J. 2001 Jun 1;356(Pt 2):487-93. doi: 10.1042/0264-6021:3560487.
The inactivation process of native (N) human butyrylcholinesterase (BuChE) by pressure and/or heat was found to be multi-step. It led to irreversible formation of an active intermediate (I) state and a denatured state. This series-inactivation process was described by expanding the Lumry-Eyring [Lumry, R. and Eyring, H. (1954) J. Phys. Chem. 58, 110-120] model. The intermediate state (I) was found to have a K(m) identical with that of the native state and a turnover rate (k(cat)) twofold higher than that of the native state with butyrylthiocholine as the substrate. The increased catalytic efficiency (k(cat)/K(m)) of I can be explained by a conformational change in the active-site gorge and/or restructuring of the water-molecule network in the active-site pocket, making the catalytic steps faster. However, a pressure/heat-induced covalent modification of native BuChE, affecting the catalytic machinery, cannot be ruled out. The inactivation process of BuChE induced by the combined action of pressure and heat was found to continue after interruption of pressure/temperature treatment. This secondary inactivation process was termed 'remnant inactivation'. We hypothesized that N and I were in equilibrium with populated metastable N' and I' states. The N' and I' states can either return to the active forms, N and I, or develop into inactive forms, N(')(in) and I(')(in). Both active N' and I' intermediate states displayed different rates of remnant inactivation depending on the pressure and temperature pretreatments and on the storage temperature. A first-order deactivation model describing the kinetics of the remnant inactivation of BuChE is proposed.
研究发现,天然(N)型人丁酰胆碱酯酶(BuChE)的压力和/或热失活过程是多步骤的。它导致了活性中间体(I)状态和变性状态的不可逆形成。通过扩展Lumry-Eyring [Lumry, R.和Eyring, H. (1954) J. Phys. Chem. 58, 110 - 120]模型来描述这一系列失活过程。发现中间体状态(I)的米氏常数(K(m))与天然状态相同,以丁酰硫代胆碱为底物时的周转速率(k(cat))比天然状态高两倍。I的催化效率(k(cat)/K(m))提高可通过活性位点峡谷的构象变化和/或活性位点口袋中水分子网络的重组来解释,这使得催化步骤更快。然而,不能排除压力/热诱导的天然BuChE的共价修饰会影响催化机制。发现压力和热联合作用诱导的BuChE失活过程在压力/温度处理中断后仍会继续。这种二次失活过程被称为“残余失活”。我们假设N和I与大量的亚稳态N'和I'处于平衡状态。N'和I'状态既可以恢复到活性形式N和I,也可以发展为非活性形式N(')(in)和I(')(in)。活性N'和I'中间体状态的残余失活速率不同,这取决于压力和温度预处理以及储存温度。提出了一个描述BuChE残余失活动力学的一级失活模型。