Cryo-EM shows stages of initial codon selection on the ribosome by aa-tRNA in ternary complex with GTP and the GTPase-deficient EF-TuH84A

Marcus Fislage, Jingji Zhang, Zuben Patrick Brown, Chandra Sekhar Mandava, Suparna Sanyal, Måns Ehrenberg, Joachim Frank

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

The GTPase EF-Tu in ternary complex with GTP and aminoacyl-tRNA (aa-tRNA) promotes rapid and accurate delivery of cognate aa-tRNAs to the ribosomal A site. Here we used cryo-EM to study the molecular origins of the accuracy of ribosome-aided recognition of a cognate ternary complex and the accuracyamplifying role of themonitoring bases A1492, A1493 and G530 of the 16S rRNA. We used the GTPasedeficient EF-Tu variant H84A with native GTP, rather than non-cleavable GTP analogues, to trap a nearcognate ternary complex in high-resolution ribosomal complexes of varying codon-recognition accuracy. We found that ribosome complexes trapped by GTPase-deficicent ternary complex due to the presence of EF-TuH84A or non-cleavable GTP analogues have very similar structures. We further discuss speed and accuracy of initial aa-tRNA selection in terms of conformational changes of aa-tRNA and stepwise activation of the monitoring bases at the decoding center of the ribosome.

Original languageEnglish
Pages (from-to)5861–5874
Number of pages14
JournalNucleic Acids Research
Volume46
Issue number11
DOIs
Publication statusPublished - 4 May 2018

Keywords

  • Codon
  • Cryoelectron Microscopy
  • Guanosine Triphosphate/chemistry
  • Models, Molecular
  • Mutation
  • Peptide Elongation Factor Tu/chemistry
  • RNA, Messenger/chemistry
  • RNA, Ribosomal, 16S/chemistry
  • RNA, Transfer, Amino Acyl/chemistry
  • Ribosomes/chemistry

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