Key result
Elongation factor G accelerates translocation by promoting steps that lead to GTPase-dependent ribosome unlocking, facilitating the formation of the rotated state and uncoupling backward motions.
This perspective highlights how EF-G and GTP hydrolysis coordinate ribosomal subunit motions to facilitate tRNA-mRNA translocation.
EF-G coordination of ribosomal motions may refine translation models; leaves open validation in eukaryotic and cardiovascular contexts.
In each round of translation elongation, tRNAs and mRNA move within the ribosome by one codon at a time. tRNA-mRNA translocation is promoted by elongation factor G (EF-G) at the cost of GTP hydrolysis. The key questions for understanding translocation are how and when the tRNAs move and how EF-G coordinates motions of the ribosomal subunits with tRNA movement. Here we present 2 recent papers which describe the choreography of movements over the whole trajectory of translocation. We present the view that EF-G accelerates translocation by promoting the steps that lead to GTPase-dependent ribosome unlocking. EF-G facilitates the formation of the rotated state of the ribosome and uncouples the backward motions of the ribosomal subunits, forming an open conformation in which the tRNAs can rapidly move. Ribosome dynamics are important not only in translocation, but also in recoding events, such as frameshifting and bypassing, and mediate sensitivity to antibiotics.
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Belardinelli et al. (2016) conducted a review in Translation elongation (basic science). Elongation factor G (EF-G) was evaluated. Elongation factor G accelerates translocation by promoting steps that lead to GTPase-dependent ribosome unlocking, facilitating the formation of the rotated state and uncoupling backward motions.
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