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8BHN

Elongating E. coli 70S ribosome containing deacylated tRNA(iMet) in the P-site and m6AAA mRNA codon with cognate dipeptidyl-tRNA(Lys) in the A-site

This is a non-PDB format compatible entry.
Summary for 8BHN
Entry DOI10.2210/pdb8bhn/pdb
Related8BF7 8BGE 8BGH 8BH4 8BHJ 8BHL
EMDB information16015 16029 16031 16047 16057 16059 16062
Descriptor50S ribosomal protein L2, 50S ribosomal protein L16, 50S ribosomal protein L17, ... (56 entities in total)
Functional Keywordsm6a, mrna modification, trna recognition, translation
Biological sourceEscherichia coli K-12
More
Total number of polymer chains56
Total formula weight2199037.25
Authors
Koziej, L.,Glatt, S. (deposition date: 2022-10-31, release date: 2023-08-16, Last modification date: 2024-10-16)
Primary citationJain, S.,Koziej, L.,Poulis, P.,Kaczmarczyk, I.,Gaik, M.,Rawski, M.,Ranjan, N.,Glatt, S.,Rodnina, M.V.
Modulation of translational decoding by m 6 A modification of mRNA.
Nat Commun, 14:4784-4784, 2023
Cited by
PubMed Abstract: N-methyladenosine (mA) is an abundant, dynamic mRNA modification that regulates key steps of cellular mRNA metabolism. mA in the mRNA coding regions inhibits translation elongation. Here, we show how mA modulates decoding in the bacterial translation system using a combination of rapid kinetics, smFRET and single-particle cryo-EM. We show that, while the modification does not impair the initial binding of aminoacyl-tRNA to the ribosome, in the presence of mA fewer ribosomes complete the decoding process due to the lower stability of the complexes and enhanced tRNA drop-off. The mRNA codon adopts a π-stacked codon conformation that is remodeled upon aminoacyl-tRNA binding. mA does not exclude canonical codon-anticodon geometry, but favors alternative more dynamic conformations that are rejected by the ribosome. These results highlight how modifications outside the Watson-Crick edge can still interfere with codon-anticodon base pairing and complex recognition by the ribosome, thereby modulating the translational efficiency of modified mRNAs.
PubMed: 37553384
DOI: 10.1038/s41467-023-40422-7
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.85 Å)
Structure validation

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