Holst-Hansen P, Kildsgaard J, MacDougall J, Palacios Moreno J M, Egebjerg J, Mortensen K K, Sperling-Petersen H U
Department of Molecular and Structural Biology, Aarhus University, Aarhus C, Denmark.
Biochimie. 1997 Dec;79(12):725-9. doi: 10.1016/s0300-9084(97)86930-1.
Polypeptide chain termination in Escherichia coli is known to require two codon specific release factors, RF1 and RF2. A third factor, RF3, has been described to stimulate the termination. Earlier investigations have estimated the cellular content of factors RF1 and RF2. Two different immunological techniques for measuring the amount of RF3 per cell in crude E coli cell extracts are reported here, using a sensitive immunoblotting method and a sandwich assay by ELISA. Monoclonal murine antibodies and polyclonal rabbit antibodies were raised against extensively purified recombinant E coli RF3. The immunoblotting involves a specific monoclonal antibody (mAb), biotinylated second antibody and finally radioactive iodinated streptavidin. In the sandwich assay polyclonal antibodies are immobilised on a polystyrene surface before addition of crude cell extract; a specific mAb serves as primary antibody and an HRP-labelled anti-mouse Ig as secondary antibody. Both methods are accurate and rapid to perform. The number of RF3 molecules per cell in exponentially growing E coli cells was found to vary considerably according to the K12 strain examined and depended on the culture medium (from 20 to 500 molecules per cell), faster growth being positively correlated with the number of RF3 molecules per cell.
已知大肠杆菌中的多肽链终止需要两种密码子特异性释放因子,即RF1和RF2。已经描述了第三种因子RF3可刺激终止过程。早期研究估计了因子RF1和RF2的细胞含量。本文报道了两种不同的免疫技术,用于使用灵敏的免疫印迹法和ELISA夹心测定法来测量大肠杆菌粗细胞提取物中每个细胞的RF3含量。针对广泛纯化的重组大肠杆菌RF3制备了单克隆鼠抗体和多克隆兔抗体。免疫印迹法涉及一种特异性单克隆抗体(mAb)、生物素化二抗以及最后放射性碘化抗生物素蛋白链菌素。在夹心测定法中,在加入粗细胞提取物之前,将多克隆抗体固定在聚苯乙烯表面;一种特异性单克隆抗体用作一抗,而辣根过氧化物酶标记的抗小鼠Ig用作二抗。这两种方法执行起来都准确且快速。发现指数生长的大肠杆菌细胞中每个细胞的RF3分子数量根据所检测的K12菌株有很大差异,并且取决于培养基(每个细胞20至500个分子),生长速度越快与每个细胞的RF3分子数量呈正相关。