Zhao Qing, Ofverstedt Lars-Göran, Skoglund Ulf, Isaksson Leif A
Department of Microbiology, Stockholm University, S-106 91 Stockholm, Sweden.
Exp Cell Res. 2004 Jul 15;297(2):495-507. doi: 10.1016/j.yexcr.2004.03.049.
Cryo-electron tomography has been used to reconstruct the structures of individual ribosomal 30S subunits in Escherichia coli cells treated with rifampicin. Rifampicin inhibits transcription initiation, thus giving depletion of mRNA and accumulation of free 30S and 50S subunits in the cell. Here, we present the 3D morphologies of reconstructed individual 30S ribosomal subunits both in vitro and in situ from E. coli. The head, the platform, and the body of the structures show large conformational movements relative to each other. The particles were grouped into three conformational groups according to the ratio between width and height in the subunit solvent side view. Also, an S15 fusion protein derivative has been used as a physical reporter to localize S15 in the 30S subunit. The results demonstrate a considerable morphological heterogeneity and structural variability among 30S ribosomal subunits.
冷冻电子断层扫描已被用于重建经利福平处理的大肠杆菌细胞中单个核糖体30S亚基的结构。利福平抑制转录起始,从而导致细胞内mRNA耗尽以及游离30S和50S亚基积累。在此,我们展示了从大肠杆菌体外和原位重建的单个30S核糖体亚基的三维形态。这些结构的头部、平台和主体相对于彼此显示出较大的构象运动。根据亚基溶剂侧视图中的宽度与高度之比,将颗粒分为三个构象组。此外,一种S15融合蛋白衍生物已被用作物理报告分子来定位30S亚基中的S15。结果表明,30S核糖体亚基之间存在相当大的形态异质性和结构变异性。