Lakomek M, Tillmann W, Scharnetzky M, Schröter W, Winkler H
Enzyme. 1983;29(3):189-97.
Investigations on the activity and the kinetic behavior of red cell pyruvate kinase in the erythrocyte membrane and hemolysate of 6 patients with pyruvate kinase (PK) deficiency are presented and compared with those of normal individuals. Hemolysate: The PK in the hemolysate of normal individuals showed the well-known allosteric properties, reflected by sigmoidal reaction kinetics (Hill-coefficient greater than 1). In contrast to these findings the enzymes of 4 of the patients which had not been splenectomised and which were all in satisfactory condition showed between 15 and 35% of the PK activity of normal individuals in the hemolysates, whereas in the case of the 2 splenectomised patients only 5 and 15% of this activity could be measured. All of the patients' enzymes showed non allosteric (hyperbolic) reaction kinetics (Hill-coefficient approximately 1.0). Red cell membranes: Our studies confirmed earlier reports that not only the hemolysate of the patients, but also their red cell membranes ('ghosts') exhibit PK activity. In normal individuals the activity of the membrane-localised PK is about 5% of the cytoplasmatic one. In case of the membrane-localised enzyme of all patients--irrespective if they were splenectomised or not--the activity is decreased to 30-50%, compared to the activity of ghosts of the control persons. Reaction kinetic studies on the PK isolated from red cell membranes from normal individuals as well as from all 6 patients exhibited hyperbolic Michaelis-Menten kinetics with Hill coefficients around 1.0.
本文展示了对6例丙酮酸激酶(PK)缺乏症患者红细胞膜和溶血产物中红细胞丙酮酸激酶活性及动力学行为的研究,并与正常个体进行了比较。溶血产物:正常个体溶血产物中的PK表现出众所周知的别构特性,由S形反应动力学反映(希尔系数大于1)。与这些发现相反,4例未行脾切除术且状况良好的患者的酶在溶血产物中的PK活性仅为正常个体的15%至35%,而2例脾切除患者的该活性仅可测到5%和15%。所有患者的酶均表现出非别构(双曲线)反应动力学(希尔系数约为1.0)。红细胞膜:我们的研究证实了早期报告,即不仅患者的溶血产物,而且其红细胞膜(“血影”)也表现出PK活性。在正常个体中,膜定位的PK活性约为细胞质中PK活性的5%。对于所有患者的膜定位酶,无论是否行脾切除术,与对照者血影的活性相比,其活性均降至30%至50%。对从正常个体以及所有6例患者的红细胞膜中分离出的PK进行的反应动力学研究均显示出双曲线型米氏动力学,希尔系数约为1.0。