Yada Y, Ozeki T, Kanoh H, Nozawa Y
Department of Biochemistry, Gifu University School of Medicine, Japan.
J Biol Chem. 1990 Nov 5;265(31):19237-43.
Three isozymes of diacylglycerol kinase (DGK), DGK-I, DGK-II, and DGK-III, were purified from the cytosol of human platelets by successive chromatography on DEAE-cellulose, Ultrogel AcA34, heparin-Sepharose, ATP-agarose, Mono Q, phenyl-Superose, HCA-hydroxyapatite, Wakopak G40, and TSK-3000SW columns. Two DGK species (DGK-I and DGK-III) were purified to apparent homogeneity, and upon SDS-polyacrylamide gel electrophoresis, they showed a single band of apparent molecular mass of 152 kDa (DGK-I) or 58 kDa (DGK-III). The peptide mapping analysis showed that DGK-I and DGK-III are structurally different. DGK-II was only partially purified, and its apparent Mr was estimated to be 75,000 by gel filtration. The specific enzyme activities of the three isozymes were increased 1,480-fold (DGK-I), 690-fold (DGK-II) and 2,100-fold (DGK-III) over original platelet cytosol. The activities of DGK-II and DGK-III were markedly enhanced by the presence of deoxycholate or phosphatidylserine, whereas DGK-I activity was not much affected by the anionic compounds. All of the three activities were strongly suppressed by phosphatidylcholine. Triton X-100 and octyl glucoside were strongly inhibitory to all of the enzymes, although to different extents. The DGK inhibitor, R59022, inhibited DGK-II and to a lesser extent DGK-III, but little affected DGK-I activity. DGK-I was much more heat-stable than DGK-II and DGK-III. The Km values for ATP were 150 microM for DGK-I, 245 microM for DGK-II, and 450 microM for DGK-III. The apparent Km values for suspended diolein were not much different among the DGKs and were in the range of 50-80 microM. These observations indicate that human platelet cytosol contains DGK isozymes with different enzymological properties. Furthermore, the three DGKs isolated from human platelets were found not to cross-react with the antibody raised against porcine brain 80-kDa DGK, thus indicating that human platelets contain novel species of DGK.
通过在DEAE-纤维素、Ultrogel AcA34、肝素-琼脂糖、ATP-琼脂糖、Mono Q、苯基-超级琼脂糖、HCA-羟基磷灰石、Wakopak G40和TSK-3000SW柱上连续层析,从人血小板的胞质溶胶中纯化出二酰基甘油激酶(DGK)的三种同工酶,即DGK-I、DGK-II和DGK-III。两种DGK同工酶(DGK-I和DGK-III)被纯化至表观均一,在SDS-聚丙烯酰胺凝胶电泳上,它们显示出一条表观分子量为152 kDa(DGK-I)或58 kDa(DGK-III)的单一条带。肽图谱分析表明DGK-I和DGK-III在结构上不同。DGK-II仅被部分纯化,通过凝胶过滤估计其表观Mr为75,000。三种同工酶的比酶活性相对于原始血小板胞质溶胶分别增加了1480倍(DGK-I)、690倍(DGK-II)和2100倍(DGK-III)。脱氧胆酸盐或磷脂酰丝氨酸的存在显著增强了DGK-II和DGK-III的活性,而DGK-I的活性受这些阴离子化合物的影响不大。三种活性均被磷脂酰胆碱强烈抑制。Triton X-100和辛基葡糖苷对所有酶均有强烈抑制作用,尽管程度不同。DGK抑制剂R59022抑制DGK-II,对DGK-III的抑制作用较小,但对DGK-I的活性影响不大。DGK-I比DGK-II和DGK-III更耐热。DGK-I对ATP的Km值为150 microM,DGK-II为245 microM,DGK-III为450 microM。三种DGK对悬浮二油精的表观Km值差异不大,在50 - 80 microM范围内。这些观察结果表明人血小板胞质溶胶含有具有不同酶学性质的DGK同工酶。此外,从人血小板中分离出的三种DGK被发现与针对猪脑80 kDa DGK产生的抗体不发生交叉反应,因此表明人血小板含有新型的DGK。