Teraoka H, Tsukada K
J Biol Chem. 1985 Mar 10;260(5):2937-40.
A monospecific antibody against calf thymus DNA ligase composed of a single polypeptide with Mr = 130,000 cross-reacts with rodent and calf thymus DNA ligases. The antibody precipitates a single Mr = 200,000 polypeptide from detergent lysates of [3H] leucine-labeled mouse Ehrlich tumor cells and calf thymocytes. Pulse-chase experiments show that the Mr = 200,000 polypeptide in Ehrlich tumor cells has a half-life of about 0.5 h. In addition to the Mr = 200,000 polypeptide, a Mr = 130,000 polypeptide is detected in the partially purified enzyme preparations from radiolabeled Ehrlich tumor cells. These results suggest that DNA ligase is synthesized in mammalian cells as a Mr = 200,000 polypeptide and that the Mr = 200,000 polypeptide is degraded to a Mr = 130,000 polypeptide by a limited proteolysis in vitro.
一种针对小牛胸腺DNA连接酶的单特异性抗体,由一条分子量为130,000的单一多肽组成,可与啮齿动物和小牛胸腺DNA连接酶发生交叉反应。该抗体从[³H]亮氨酸标记的小鼠艾氏瘤细胞和小牛胸腺细胞的去污剂裂解物中沉淀出一条分子量为200,000的单一多肽。脉冲追踪实验表明,艾氏瘤细胞中分子量为200,000的多肽半衰期约为0.5小时。除了分子量为200,000的多肽外,在来自放射性标记的艾氏瘤细胞的部分纯化酶制剂中还检测到一条分子量为130,000的多肽。这些结果表明,DNA连接酶在哺乳动物细胞中以分子量为200,000的多肽形式合成,并且分子量为200,000的多肽在体外通过有限的蛋白水解作用降解为分子量为130,000的多肽。