Key result
Translational elongation factor G functions as a force-generating mechanochemical device rather than a simple conformational switch to power the directional movement of mRNA and tRNAs on the ribosome.
Proposes a model where EF-G acts as a mechanochemical motor, similar to myosin, to drive ribosomal translocation.
This mechanochemical EF-G model may guide ribosome research; leaves open validation across systems.
EF-G is a large, five-domain GTPase that promotes the directional movement of mRNA and tRNAs on the ribosome in a GTP-dependent manner. Unlike other GTPases, but by analogy to the myosin motor, EF-G performs its function of powering translocation in the GDP-bound form; that is, in a kinetically stable ribosome-EF-G(GDP) complex formed by GTP hydrolysis on the ribosome. The complex undergoes an extensive structural rearrangement, in particular affecting the small ribosomal subunit, which leads to mRNA-tRNA movement. Domain 4, which extends from the 'body' of the EF-G molecule much like a lever arm, appears to be essential for the structural transition to take place. In a hypothetical model, GTP hydrolysis induces a conformational change in the G domain of EF-G which affects the interactions with neighbouring domains within EF-G. The resulting rearrangement of the domains relative to each other generates conformational strain in the ribosome to which EF-G is fixed. Because of structural features of the tRNA-ribosome complex, this conformational strain results in directional tRNA-mRNA movement. The functional parallels between EF-G and motor proteins suggest that EF-G differs from classical G-proteins in that it functions as a force-generating mechanochemical device rather than a conformational switch. There are other multi-domain GTPases that may function in a similar way.
No takes yet. Share an insight, caveat, or question.
Wintermeyer et al. (2000) reported a review. Translational elongation factor G functions as a force-generating mechanochemical device rather than a simple conformational switch to power the directional movement of mRNA and tRNAs on the ribosome.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: