Large-scale movements of IF3 and tRNA during bacterial translation initiation

• Tanweer Hussain ; José Luis Llàcer ^[1] ; Brian T. Wimberly ^[1]
  1. [1] MRC Laboratory of Molecular Biology

     MRC Laboratory of Molecular Biology

     Cambridge District, Reino Unido

     
• Localización: Cell, ISSN 0092-8674, Vol. 167, Nº. 1, 2016, págs. 133-144
• Idioma: inglés
• Texto completo no disponible (Saber más ...)
• Resumen

  • In bacterial translational initiation, three initiation factors (IFs 1–3) enable the selection of initiator tRNA and the start codon in the P site of the 30S ribosomal subunit. Here, we report 11 single-particle cryo-electron microscopy (cryoEM) reconstructions of the complex of bacterial 30S subunit with initiator tRNA, mRNA, and IFs 1–3, representing different steps along the initiation pathway. IF1 provides key anchoring points for IF2 and IF3, thereby enhancing their activities. IF2 positions a domain in an extended conformation appropriate for capturing the formylmethionyl moiety charged on tRNA. IF3 and tRNA undergo large conformational changes to facilitate the accommodation of the formylmethionyl-tRNA (fMet-tRNAfMet) into the P site for start codon recognition.