| Literature DB >> 27063503 |
Enea Salsi1, Elie Farah1, Dmitri N Ermolenko2.
Abstract
Elongation factor G (EF-G) is a universally conserved translational GTPase that promotes the translocation of tRNA and mRNA through the ribosome. EF-G binds to the ribosome in a GTP-bound form and subsequently catalyzes GTP hydrolysis. The contribution of the ribosome-stimulated GTP hydrolysis by EF-G to tRNA/mRNA translocation remains debated. Here, we show that while EF-G•GDP does not stably bind to the ribosome and induce translocation, EF-G•GDP in complex with phosphate group analogs BeF3(-) and AlF4(-) promotes the translocation of tRNA and mRNA. Furthermore, the rates of mRNA translocation induced by EF-G in the presence of GTP and a non-hydrolyzable analog of GTP, GDP•BeF3(-) are similar. Our results are consistent with the model suggesting that GTP hydrolysis is not directly coupled to mRNA/tRNA translocation. Hence, GTP binding is required to induce the activated, translocation-competent conformation of EF-G while GTP hydrolysis triggers EF-G release from the ribosome.Entities:
Keywords: Beryllium fluoride; EF-G; GTP hydrolysis; Ribosome; mRNA translocation
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Year: 2016 PMID: 27063503 PMCID: PMC4884529 DOI: 10.1016/j.jmb.2016.03.032
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469