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 language | English |
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Pages (from-to) | 5861–5874 |
Number of pages | 14 |
Journal | Nucleic Acids Research |
Volume | 46 |
Issue number | 11 |
DOIs | |
Publication status | Published - 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