The structure of helix 89 of 23S rRNA is important for peptidyl transferase function of Escherichia coli ribosome

Dmitry E. Burakovsky, Petr V. Sergiev, Maria A. Steblyanko, Andrey L. Konevega, Alexey A. Bogdanov, Olga A. Dontsova

Research output: Contribution to journalArticlepeer-review

18 Citations (Scopus)

Abstract

Helix 89 of the 23S rRNA connects ribosomal peptidyltransferase center and elongation factor binding site. Secondary structure of helix 89 determined by X-ray structural analysis involves less base pairs then could be drawn for the helix of the same primary structure. It can be that alternative secondary structure might be realized at some stage of translation. Here by means of site-directed mutagenesis we stabilized either the "X-ray" structure or the structure with largest number of paired nucleotides. Mutation UU2492-3C which aimed to provide maximal pairing of the helix 89 of the 23S rRNA was lethal. Mutant ribosomes were unable to catalyze peptide transfer independently either with aminoacyl-tRNA or puromycin.

Original languageEnglish
Pages (from-to)3073-3078
Number of pages6
JournalFEBS Letters
Volume585
Issue number19
DOIs
Publication statusPublished - 3 Oct 2011
Externally publishedYes

Keywords

  • Mutagenesis
  • Peptidyltransferase
  • Ribosome
  • rRNA

Fingerprint

Dive into the research topics of 'The structure of helix 89 of 23S rRNA is important for peptidyl transferase function of Escherichia coli ribosome'. Together they form a unique fingerprint.

Cite this