Volume 18, Issue 6, Pages (June 2010)

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Volume 18, Issue 6, Pages 719-724 (June 2010) Structure of the 100S Ribosome in the Hibernation Stage Revealed by Electron Cryomicroscopy  Takayuki Kato, Hideji Yoshida, Tomoko Miyata, Yasushi Maki, Akira Wada, Keiichi Namba  Structure  Volume 18, Issue 6, Pages 719-724 (June 2010) DOI: 10.1016/j.str.2010.02.017 Copyright © 2010 Elsevier Ltd Terms and Conditions

Structure 2010 18, 719-724DOI: (10.1016/j.str.2010.02.017) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 1 Electron Cryomicrographs of Frozen-Hydrated 100S Ribosomes and Averaged Image (A) Noncrosslinked (left) and crosslinked (right) specimens. Red circles and yellow ellipses indicate monomer and dimer ribosomes, respectively. The scale bar represents 50 nm. (B) Average of 1156 particle images in one of the 40 different classes (Figure S1). The scale bar represents 20 nm. Structure 2010 18, 719-724DOI: (10.1016/j.str.2010.02.017) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 2 3D Density Map of a 70S Ribosome with Part of Its Partner in the 100S Ribosome (A) The 50S and 30S subunits of a 70S ribosome and an extra density paired with the 30S subunit are colored cyan, yellow, and light green, respectively. (B) Cross-section showing the tRNA-free interface between the 50S and 30S subunits. The locations of the tRNA at the A-, P-, and E-site are indicated by the red, green, and yellow ribbon models, respectively. The scale bar represents 20 nm. Domains and proteins are labeled as: CP, central protuberance; L1, L1 protein of the 50S subunit; St, L7/L12 stalk; hd, head; bk, beak; sp, spur. Structure 2010 18, 719-724DOI: (10.1016/j.str.2010.02.017) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 3 Model of the 100S Ribosome with a Two-Fold Symmetry The 50S subunits are colored cyan and pink, and the 30S subunits are colored yellow and green. The two-fold symmetry axis is indicated in pink in the right panel. The arrows indicate the extra density unoccupied by any known component proteins of the ribosome. The black and red dots in the right panel indicate the position of S6 and S18, respectively. Domain labels not shown in Figure 2 are: bd, body; pt, platform. Structure 2010 18, 719-724DOI: (10.1016/j.str.2010.02.017) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 4 Contact Point between the 70S Ribosomes (A) Paired 30S subunits are colored yellow and green. (B) The slab of the part indicated by the box in (A) is viewed in stereo, in the same direction as in (A) in the upper panel and in the direction of the arrow in (A) in the lower panel, to show the S2-S5 contact region more clearly. The S2, S3, S4, and S5 proteins are shown by the orange, pink, purple, and cyan ribbon models, respectively. Two α helices of S3 (residues 107–126 and 128–142) and one α helix of S5 (residues 54–68) are colored red and dark green, respectively. Domain labels are the same as in Figures 2 and 3. Structure 2010 18, 719-724DOI: (10.1016/j.str.2010.02.017) Copyright © 2010 Elsevier Ltd Terms and Conditions

Figure 5 Schematic Diagram Showing the Formation Process of the 100S Ribosome upon Transition from the Log Phase to the Stationary Growth Phase Protein factors involved in the process are: RRF, ribosome recycling factor; EF-G, elongation factor G; RMF, ribosome modulation factor; HPF, hibernation promoting factor. Structure 2010 18, 719-724DOI: (10.1016/j.str.2010.02.017) Copyright © 2010 Elsevier Ltd Terms and Conditions