Samenvatting
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.
Originele taal-2 | English |
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Pagina's (van-tot) | 5861–5874 |
Aantal pagina's | 14 |
Tijdschrift | Nucleic Acids Research |
Volume | 46 |
Nummer van het tijdschrift | 11 |
DOI's | |
Status | Published - 4 mei 2018 |