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Cryo-EM structure of the mammalian eukaryotic release factor eRF1-eRF3-associated termination complex

  • Derek Taylor
  • , Anett Unbehaun
  • , Wen Li
  • , Sanchaita Das
  • , Jianlin Lei
  • , Hstau Y. Liao
  • , Robert A. Grassucci
  • , Tatyana V. Pestova
  • , Joachim Frank
  • Case Western Reserve University
  • SUNY Downstate Health Sciences University
  • Charité – Universitätsmedizin Berlin
  • Columbia University
  • Tsinghua University

Research output: Contribution to journalArticlepeer-review

59 Scopus citations

Abstract

Eukaryotic translation termination results from the complex functional interplay between two eukaryotic release factors, eRF1 and eRF3, and the ribosome, in which GTP hydrolysis by eRF3 couples codon recognition with peptidyl-tRNA hydrolysis by eRF1. Here, using cryo-electron microscopy (cryo-EM) and flexible fitting, we determined the structure of eRF1-eRF3-guanosine 5′-[β,γ-imido] triphosphate (GMPPNP)-bound ribosomal pretermination complex (pre-TC), which corresponds to the initial, pre-GTP hydrolysis stage of factor attachment. Our results show that eukaryotic translation termination involves a network of interactions between the two release factors and the ribosome. Our structure provides mechanistic insight into the coordination between GTP hydrolysis by eRF3 and subsequent peptide release by eRF1.

Original languageEnglish
Pages (from-to)18413-18418
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume109
Issue number45
DOIs
StatePublished - Nov 6 2012

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