Stöffler-Meilicke M, Stöffler G
Max-Planck-Institut für Molekulare Genetik, Abt Wittmann, Berlin, Dahlem, Germany.
Biochimie. 1991 Jun;73(6):797-804. doi: 10.1016/0300-9084(91)90059-a.
It has been shown by electron microscopy that the selective removal of the stalk from 50S ribosomal subunits of two representative archaebacteria, namely Methanococcus vaniellii and Sulfolobus solfataricus, is accompanied by loss of the archaebacterial L10 and L12 proteins. The stalk was reformed if archaebacterial core particles were reconstituted with their corresponding split proteins. Next, structurally intact chimeric 50S subunits have been reconstituted in vitro by addition of Escherichia coli ribosomal proteins L10 and L7/L12 to 50S core particles from M vaniellii or S solfataricus, respectively. In the reverse experiment, using core particles from E coli and split proteins from M vaniellii, stalk-bearing 50S particles were also obtained. Analysis of the reconstituted 50S subunits by immunoblotting revealed that E coli L10 was incorporated into archaebacterial core particles in both presence or absence of E coli L7/L12. In contrast, incorporation of E coli L7/L12 into archaebacterial cores was only possible in the presence of E coli L10. Our results suggest that in archaebacteria - as in E coli - the stalk is formed by archaebacterial L12 proteins that bind to the ribosome via L10. The structural equivalence of eubacterial and archaebacterial L10 and L12 proteins has thus for the first time been established. The chimeric reconstitution experiments provide evidence that the domain of protein L10 that interacts with the ribosomal particle is highly conserved between eubacteria and archaebacteria.
电子显微镜研究表明,从两种代表性古细菌,即万氏甲烷球菌和嗜热栖热菌的50S核糖体亚基中选择性去除柄部,会伴随着古细菌L10和L12蛋白的丢失。如果用相应的裂解蛋白重构古细菌核心颗粒,柄部会重新形成。接下来,通过分别向来自万氏甲烷球菌或嗜热栖热菌的50S核心颗粒中添加大肠杆菌核糖体蛋白L10和L7/L12,在体外重构了结构完整的嵌合50S亚基。在反向实验中,使用来自大肠杆菌的核心颗粒和来自万氏甲烷球菌的裂解蛋白,也获得了带有柄部的50S颗粒。通过免疫印迹分析重构的50S亚基发现,无论有无大肠杆菌L7/L12,大肠杆菌L10都能掺入古细菌核心颗粒中。相比之下,只有在存在大肠杆菌L10的情况下,大肠杆菌L7/L12才能掺入古细菌核心中。我们的结果表明,在古细菌中——与在大肠杆菌中一样——柄部由通过L10与核糖体结合的古细菌L12蛋白形成。因此,首次确立了真细菌和古细菌L10和L12蛋白在结构上的等效性。嵌合重构实验提供了证据,表明蛋白L10与核糖体颗粒相互作用的结构域在真细菌和古细菌之间高度保守。