4.7 Article

Visualization of the eEF2-80S ribosome transition-state complex by cryo-electron microscopy

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 382, Issue 1, Pages 179-187

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2008.07.004

Keywords

AlF4-; GDP; GTPase; ribosome; translocation

Funding

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM055440, R01 GM055440-14, R37 GM029169, R01-GM-55440] Funding Source: Medline

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In an attempt to understand ribosome-induced GTP hydrolysis on eEF2, we determined a 12.6-angstrom cryo-electron microscopy reconstruction of the eEF2-bound 80S ribosome in the presence of aluminum tetrafluoride and GDP, with aluminum tetrafluoride mimicking the gamma-phosphate during hydrolysis. This is the first visualization of a structure representing a transitionstate complex on the ribosome. Tight interactions are observed between the factor's G domain and the large ribosomal subunit, as well as between domain IV and an intersubunit bridge. In contrast, some of the domains of eEF2 implicated in small subunit binding display a large degree of flexibility. Furthermore, we find support for a transition-state model conformation of the switch I region in this complex where the reoriented switch I region interacts with a conserved rRNA region of the 40S subunit formed by loops of the 18S RNA helices 8 and 14. This complex is structurally distinct from the eEF2-bound 80S ribosome complexes previously reported, and analysis of this map sheds light on the GTPase-coupled translocation mechanism. (C) 2008 Elsevier Ltd. All rights reserved.

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