Nierhaus K H, Montejo V
Proc Natl Acad Sci U S A. 1973 Jul;70(7):1931-5. doi: 10.1073/pnas.70.7.1931.
Cores were prepared from 50S ribosomal subunits by incubation with 0.4 M LiCl/Mg(++) (0.4c cores); 0.8c cores and corresponding SP(0.4-0.8) split proteins were obtained from 0.4c cores. In the fragment reaction 0.4c cores were active, but 0.8c cores were not. Activity of the 0.8c cores could be restored by reconstitution with the SP(0.4-0.8) fraction. The split proteins were separated by DEAE-cellulose chromatography and Sephadex gel filtration. The peptidyltransferase activity is correlated with the amount of protein L11 added to the 0.8c core under reconstitution conditions. Whether protein L11 displays the enzymatic activity itself or is part of the enzymatic center is discussed.
通过与0.4M LiCl/Mg(++)(0.4c核心)孵育从50S核糖体亚基制备核心;从0.4c核心获得0.8c核心和相应的SP(0.4 - 0.8)分裂蛋白。在片段反应中,0.4c核心具有活性,但0.8c核心没有。用SP(0.4 - 0.8)组分重构可恢复0.8c核心的活性。通过DEAE - 纤维素色谱和Sephadex凝胶过滤分离分裂蛋白。肽基转移酶活性与在重构条件下添加到0.8c核心的L11蛋白量相关。讨论了L11蛋白本身是否具有酶活性或是否是酶中心的一部分。