Summary information and primary citation
- PDB-id
-
4v8d;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- ribosome
- Method
- X-ray (3.0 Å)
- Summary
- Structure analysis of ribosomal decoding (cognate
trna-tyr complex).
- Reference
-
Demeshkina N, Jenner L, Westhof E, Yusupov M, Yusupova G
(2012): "A new
understanding of the decoding principle on the
ribosome." Nature, 484,
256-259. doi: 10.1038/nature10913.
- Abstract
- During protein synthesis, the ribosome accurately
selects transfer RNAs (tRNAs) in accordance with the
messenger RNA (mRNA) triplet in the decoding centre. tRNA
selection is initiated by elongation factor Tu, which
delivers tRNA to the aminoacyl tRNA-binding site (A site)
and hydrolyses GTP upon establishing codon-anticodon
interactions in the decoding centre. At the following
proofreading step the ribosome re-examines the tRNA and
rejects it if it does not match the A codon. It was
suggested that universally conserved G530, A1492 and A1493
of 16S ribosomal RNA, critical for tRNA binding in the A
site, actively monitor cognate tRNA, and that recognition
of the correct codon-anticodon duplex induces an overall
ribosome conformational change (domain closure). Here we
propose an integrated mechanism for decoding based on six
X-ray structures of the 70S ribosome determined at
3.1-3.4 Å resolution, modelling cognate or near-cognate
states of the decoding centre at the proofreading step. We
show that the 30S subunit undergoes an identical domain
closure upon binding of either cognate or near-cognate
tRNA. This conformational change of the 30S subunit forms a
decoding centre that constrains the mRNA in such a way that
the first two nucleotides of the A codon are limited to
form Watson-Crick base pairs. When U·G and G·U mismatches,
generally considered to form wobble base pairs, are at the
first or second codon-anticodon position, the decoding
centre forces this pair to adopt the geometry close to that
of a canonical C·G pair. This by itself, or with
distortions in the codon-anticodon mini-helix and the
anticodon loop, causes the near-cognate tRNA to dissociate
from the ribosome.