Tokunaga M, Kawamura A, Kohno K
Laboratory of Molecular Genetics, Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
J Biol Chem. 1992 Sep 5;267(25):17553-9.
Using specific anti-BiP/Kar2 antibody as the probe, we have developed an efficient purification method of BiP/Kar2 protein from the total cell extract of Saccharomyces cerevisiae. Overproduction of BiP/Kar2 protein was achieved by the cloning of the KAR2 gene on multicopy plasmids and the treatment of cells harboring the cloned KAR2 gene with tunicamycin. Freeze-thaw treatment, hydroxyapatite high pressure liquid chromatography, and ATP-agarose column chromatography of crude extract yielded homogeneous BiP/Kar2 protein (including less than 0.2% of degradative derivative) with a 430-fold purification and 28% recovery. Edman degradation of purified BiP/Kar2 suggests that the mature protein corresponds to a processed product with the removal of a 42-amino acid presequence. It is active as a homodimer and exhibits ATPase activity with a specific activity of 2 pmol/min/micrograms of protein. Protease susceptibility indicated that the ADP form of BiP/Kar2 is more resistant than the ATP form to the chymotrypsin digestion and that BiP/Kar2 required the presence of ATP to avoid the irreversible denaturation. Synthesis of BiP/Kar2 was induced by the inducible expression of an aberrant heterologous protein, yeast killer prepro-signal mouse alpha-amylase fusion protein.
以特异性抗BiP/Kar2抗体作为探针,我们开发了一种从酿酒酵母全细胞提取物中高效纯化BiP/Kar2蛋白的方法。通过将KAR2基因克隆到多拷贝质粒上,并对携带克隆KAR2基因的细胞用衣霉素处理,实现了BiP/Kar2蛋白的过量表达。对粗提取物进行冻融处理、羟基磷灰石高压液相色谱和ATP-琼脂糖柱色谱,得到了均一的BiP/Kar2蛋白(包括少于0.2%的降解衍生物),纯化倍数为430倍,回收率为28%。对纯化的BiP/Kar2进行埃德曼降解表明,成熟蛋白对应于去除了42个氨基酸前导序列的加工产物。它作为同源二聚体具有活性,表现出ATP酶活性,比活性为2 pmol/分钟/微克蛋白。蛋白酶敏感性表明,BiP/Kar2的ADP形式比ATP形式对胰凝乳蛋白酶消化更具抗性,并且BiP/Kar2需要ATP的存在以避免不可逆变性。BiP/Kar2的合成由异常异源蛋白酵母杀手前原信号小鼠α淀粉酶融合蛋白的诱导表达所诱导。