| Ribosomal Proteins S12 and S13 Function as Control Elements for Translocation of the mRNA:tRNA Complex Molecular Cell, Volume 12, Issue 2, 1 August 2003, Pages 321-328 Anthony R Cukras, Daniel R Southworth, Julie L Brunelle, Gloria M Culver and Rachel Green Summary Translocation of the mRNA:tRNA complex through the ribosome is promoted by elongation factor G (EF-G) during the translation cycle. Previous studies established that modification of ribosomal proteins with thiol-specific reagents promotes this event in the absence of EF-G. Here we identify two small subunit interface proteins S12 and S13 that are essential for maintenance of a pretranslocation state. Omission of these proteins using in vitro reconstitution procedures yields ribosomal particles that translate in the absence of enzymatic factors. Conversely, replacement of cysteine residues in these two proteins yields ribosomal particles that are refractive to stimulation with thiol-modifying reagents. These data support a model where S12 and S13 function as control elements for the more ancient rRNA- and tRNA-driven movements of translocation. Summary | Full Text | PDF (365 kb) |
| Progression of the Ribosome Recycling Factor through the Ribosome Dissociates the Two Ribosomal Subunits Molecular Cell, Volume 27, Issue 2, 20 July 2007, Pages 250-261 Chandana Barat, Partha P. Datta, V. Samuel Raj, Manjuli R. Sharma, Hideko Kaji, Akira Kaji and Rajendra K. Agrawal Summary After the termination step of translation, the posttermination complex (PoTC), composed of the ribosome, mRNA, and a deacylated tRNA, is processed by the concerted action of the ribosome-recycling factor (RRF), elongation factor G (EF-G), and GTP to prepare the ribosome for a fresh round of protein synthesis. However, the sequential steps of dissociation of the ribosomal subunits, and release of mRNA and deacylated tRNA from the PoTC, are unclear. Using three-dimensional cryo-electron microscopy, in conjunction with undecagold-labeled RRF, we show that RRF is capable of spontaneously moving from its initial binding site on the 70S ribosome to a site exclusively on the large 50S ribosomal subunit. This movement leads to disruption of crucial intersubunit bridges and thereby to the dissociation of the two ribosomal subunits, the central event in ribosome recycling. Results of this study allow us to propose a model of ribosome recycling. Summary | Full Text | PDF (1744 kb) |
| Splitting of the Posttermination Ribosome into Subunits by the Concerted Action of RRF and EF-G Molecular Cell, Volume 18, Issue 6, 10 June 2005, Pages 675-686 Andrey V. Zavialov, Vasili V. Hauryliuk and Måns Ehrenberg Summary After peptide release by a class-1 release factor, the ribosomal subunits must be recycled back to initiation. We have demonstrated that the distance between a strong Shine-Dalgarno (SD) sequence and a codon in the P site is crucial for the binding stability of the deacylated tRNA in the P site of the posttermination ribosome and the in-frame maintenance of its mRNA. We show that the elongation factor EF-G and the ribosomal recycling factor RRF split the ribosome into subunits in the absence of initiation factor 3 (IF3) by a mechanism that requires both GTP and GTP hydrolysis. Taking into account that EF-G in the GTP form and RRF bind with positive cooperativity to the free 50S subunit but with negative cooperativity to the 70S ribosome, we suggest a mechanism for ribosome recycling that specifies distinct roles for EF-G, RRF, and IF3. Summary | Full Text | PDF (580 kb) |
Copyright © 1974 The Biophysical Society. All rights reserved.
Biophysical Journal, Volume 14, Issue 7, 528-545, 1 July 1974
doi:10.1016/S0006-3495(74)85933-3
Articles
R. Gabler, E.W. Westhead and N.C. Ford
Using an optical beating technique, the diffusion coefficients and relative scattered intensity of Escherichia coli 70S, 50S, and 30S ribosomes are measured as a function of temperature and Mg2+ concentration. For solutions at 10 mM Mg2+ and between 0°C and about 40°C, the values of D20,w obtained are 1.7, 1.9, and ≈2.1×10-7 cm2/s, respectively. Preparative procedures drastically affect these values and equivalent hydrodynamic ellipsoids of revolution models give large axial ratios indicating extensive hydration or a deviation from the assumed shape. Calculations also indicate that the subunits expand upon dissociation. Measurements of D20,w vs. temperature indicate that 70S particles undergo a conformational change prior to dissociation and can be heat dissociated at 30–32°C at low concentrations. Treatment of 70S ribosomes with EDTA causes a biphasic dissociation reaction. Addition of Mg2+ after dissociation with EDTA shows that longer waiting times yield fewer 70S particles and that even short waiting times may yield ribosomes differing from the native conformation. Addition of p-chloromercuribenzoic acid (PCMB) is shown to dissociate 70S particles, but to a lesser extent than ethylenediaminetetraacetic acid (EDTA).