Hamada H, Okochi E, Oh-hara T, Tsuruo T
Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo.
Cancer Res. 1988 Jun 1;48(11):3173-8.
A low molecular weight cytoplasmic protein (Mr 19,000-22,000) has been reported to be overexpressed in some multidrug-resistant cells. We have found that a cytoplasmic protein with a molecular weight of 22,000 is highly expressed in the human myelogenous leukemia K562 cells resistant to Adriamycin (K562/ADM). The Mr 22,000 protein was shown to be one of the major calcium-binding proteins in the cytoplasmic extract from K562/ADM cells. The protein was purified to apparent homogeneity from K562/ADM cells using a four-step procedure including ammonium sulfate fractionation, anion-exchange chromatography, and gel filtration. 1.5 mg of the Mr 22,000 protein was purified from 3.0 x 10(9) of K562/ADM cells. The protein was acidic (pI 5.3) and exists as a homodimer (Mr 44,000) as revealed by gel filtration and sucrose density-gradient centrifugation. The purified protein appeared as a single band (Mr 22,000) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis in the presence or absence of reducing agents, suggesting that the homodimer was generated by noncovalent linkage. Monoclonal antibodies specific to the Mr 22,000 protein were raised by in vitro immunization with purified protein or by in vivo immunization with the crude membrane fraction of K562/ADM. These antibodies were used as probes for the detection of the protein. We have surveyed the expression of the Mr 22,000 protein in various multidrug-resistant and -sensitive cell lines, and found that the overexpression of the protein is not a sufficient nor a necessary condition for the acquisition of the multidrug-resistant phenotype.
据报道,一种低分子量的细胞质蛋白(分子量为19,000 - 22,000)在一些多药耐药细胞中过表达。我们发现,一种分子量为22,000的细胞质蛋白在对阿霉素耐药的人髓性白血病K562细胞(K562/ADM)中高度表达。该分子量为22,000的蛋白被证明是K562/ADM细胞细胞质提取物中的主要钙结合蛋白之一。使用包括硫酸铵分级分离、阴离子交换色谱和凝胶过滤在内的四步程序,从K562/ADM细胞中纯化该蛋白至表观均一。从3.0×10⁹个K562/ADM细胞中纯化得到1.5毫克分子量为22,000的蛋白。该蛋白呈酸性(pI 5.3),通过凝胶过滤和蔗糖密度梯度离心显示以同二聚体形式存在(分子量为44,000)。在有或没有还原剂存在的情况下,通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳,纯化的蛋白呈现为单一条带(分子量为22,000),表明同二聚体是由非共价连接产生的。通过用纯化蛋白进行体外免疫或用K562/ADM的粗膜部分进行体内免疫,制备了针对分子量为22,000蛋白的单克隆抗体。这些抗体用作检测该蛋白的探针。我们研究了分子量为22,000蛋白在各种多药耐药和敏感细胞系中的表达,发现该蛋白的过表达对于获得多药耐药表型既不是充分条件也不是必要条件。