Simanis V, Lane D P
Virology. 1985 Jul 15;144(1):88-100. doi: 10.1016/0042-6822(85)90308-3.
A rapid purification procedure for SV40 large T antigen has been developed which combines the use of an adenovirus-SV40 hybrid virus which overproduces large T antigen, and immunoaffinity chromatography on an anti-large T monoclonal antibody coupled to protein A Sepharose. The protein exhibits the p53-binding, ATPase, and sequence-specific DNA-binding activities of T antigen. The purification procedure can be completed in 1 day and allows the isolation of milligram amounts of large T in excellent yield. The pure protein is extremely antigenic and is tolerant of iodination to high specific activity, permitting the development of a competition radioimmunoassay for large T that reliably detects nanogram amounts of the protein.
已开发出一种用于SV40大T抗原的快速纯化程序,该程序结合使用了过量产生大T抗原的腺病毒-SV40杂交病毒,以及在与蛋白A琼脂糖偶联的抗大T单克隆抗体上进行免疫亲和层析。该蛋白具有T抗原的p53结合、ATP酶和序列特异性DNA结合活性。纯化程序可在1天内完成,并能以极高的产率分离出毫克量的大T。纯化后的蛋白具有极强的抗原性,并且耐受碘标记至高比活性,从而能够开发出一种可靠检测纳克量该蛋白的大T竞争放射免疫测定法。