Adenine phosphoribosyltransferase and hypoxanthine-guanine phosphoribosyltransferase immunoprecipitation reactions in human-mouse and human-hamster cell hybrids.

Humangenetik Pub Date : 1975-10-20 DOI:10.1007/BF00273628
K R Held, B Kahan, R DeMars
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引用次数: 4

Abstract

Male New Zealand White rabbits were immunized with human adenine phosphoribosyltransferase (APRT) and hypoxanthine-guanine phosphoribosyltransferase (HGPRT), which were purified about 2000-fold and 800-fold, respectively, from erythrocytes by DEAE-cellulose chromatography, ammonium sulfate precipitation and preparative polyacrylamide gel electrophoresis. Specific immunoprecipitations of APRT and HGPRT were achieved with the antisera that were obtained and by using polyethylene glycol as a substitute for goat anti-(rabbit) gamma globulin. The activities of the human forms of these enzymes, whether from red blood cells or from cultured cells, were almost completely eliminated under the conditions of immunoprecipitation used. Little or no reduction of APRT and HGPRT activities from mouse and Chinese hamster cells was observed. This discriminatory capacity of the antisera was successfully used for the identification of human APRT and HGPRT in human-mouse and human-hamster cell hybrids using the immunoprecipitation reaction.

腺嘌呤磷酸核糖基转移酶和次黄嘌呤-鸟嘌呤磷酸核糖基转移酶在人-小鼠和人-仓鼠杂交细胞中的免疫沉淀反应。
用人腺嘌呤磷酸核糖基转移酶(APRT)和次黄嘌呤-鸟嘌呤磷酸核糖基转移酶(HGPRT)免疫雄性新西兰大白兔,通过deae -纤维素层析、硫酸铵沉淀和制备性聚丙烯酰胺凝胶电泳分别从红细胞中纯化了约2000倍和800倍的APRT和HGPRT。用获得的抗血清和聚乙二醇作为山羊抗(兔)γ球蛋白的替代品,实现了APRT和HGPRT的特异性免疫沉淀。这些酶的人类形式的活性,无论是来自红细胞还是来自培养细胞,在使用免疫沉淀的条件下几乎完全消除。小鼠和中国仓鼠细胞的APRT和HGPRT活性几乎没有或没有降低。利用免疫沉淀反应,该抗血清的这种鉴别能力成功地用于人-小鼠和人-仓鼠杂交细胞中人APRT和HGPRT的鉴定。
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