Fujii H, Chen S H, Akatsuka J, Miwa S, Yoshida A
Proc Natl Acad Sci U S A. 1981 Apr;78(4):2587-90. doi: 10.1073/pnas.78.4.2587.
A phosphoglycerate kinase (PGKase: ATP:3-phosphoglycerate 1-phosphotransferase, EC 2.7.2.3; X chromosome-linked) variant, PGKase-Tokyo, is associated with enzyme deficiency, nonspherocytic hemolytic anemia, and neurological disturbances. Because a sufficient amount of the patient's erythrocytes was not available, the variant enzyme was purified to homogeneity from the cultured lymphoblastoid cells of the patient. The enzyme activity of the variant lymphoblastoid cells was about 16% of that of the normal lymphoblastoid cells. PGKase-Tokyo, compared to the normal enzyme, had a lower specific activity (31% of normal in the backward reaction and 15% of normal in the forward reaction), higher than normal Michaelis constants for ATP and 3-phosphoglycerate, a more acidic pH optimum, and increased thermal instability. Microscale peptide mapping analysis revealed that the structural abnormality of PGKase-Tokyo is a single amino acid substitution from valine to methionine at position 266. Thus, the use of the cultured lymphoblastoid cells is proven to be useful for the study of structural and functional abnormalities of mutant enzymes.
一种磷酸甘油酸激酶(PGKase:ATP:3 - 磷酸甘油酸1 - 磷酸转移酶,EC 2.7.2.3;X染色体连锁)变体,PGKase - 东京型,与酶缺乏、非球形红细胞溶血性贫血和神经功能障碍相关。由于无法获得足够数量的患者红细胞,因此从患者培养的淋巴母细胞中将变体酶纯化至同质状态。变体淋巴母细胞的酶活性约为正常淋巴母细胞的16%。与正常酶相比,PGKase - 东京型的比活性较低(逆向反应中为正常的31%,正向反应中为正常的15%),对ATP和3 - 磷酸甘油酸的米氏常数高于正常水平,最适pH值更偏酸性,热稳定性增加。微量肽图谱分析表明,PGKase - 东京型的结构异常是第266位的缬氨酸被甲硫氨酸单一氨基酸取代。因此,已证明培养的淋巴母细胞可用于研究突变酶的结构和功能异常。