Functional epitopes at the ribosome subunit interface
- Creators
- Rackham, Oliver
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Wang, Kaihang
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Chin, Jason W.
Abstract
The ribosome is a 2.5-MDa molecular machine that synthesizes cellular proteins encoded in mRNAs. The 30S and 50S subunits of the ribosome associate through structurally defined intersubunit bridges burying 6,000 Å^2, 80% of which is buried in conserved RNA-RNA interactions. Intersubunit bridges bind translation factors, may coordinate peptide bond formation and translocation and may be actively remodeled in the post-termination complex, but the functional importance of numerous 30S bridge nucleotides had been unknown. We carried out large-scale combinatorial mutagenesis and in vivo selections on 30S nucleotides that form RNA-RNA intersubunit bridges in the Escherichia coli ribosome. We determined the covariation and functional importance of bridge nucleotides, allowing comparison of the structural interface and phylogenetic data to the functional epitope. Our results reveal how information for ribosome function is partitioned across bridges, and suggest a subset of nucleotides that may have measurable effects on individual steps of the translational cycle.
Additional Information
© 2006 Macmillan Publishers Limited. Received 2 November 2005; accepted 14 March 2006; published online 2 April 2006. J.W.C. is an EMBO Young Investigator. K.W. is grateful for a Medical Research Council–Laboratory of Molecular Biology (MRC-LMB) Cambridge Scholarship, an Honorary External Research Studentship from Trinity College, Cambridge and an Overseas Research Studentship Award. We thank M.E. Hurles (Sanger Institute) for discussions on quantifying sequence polymorphisms, P.H. Dear (LMB) and G. Mitchison (Cambridge) for discussions on statistical methods, and T.M. Schmeing (LMB) and other members of LMB for critically reading versions of the manuscript. The authors declare no competing financial interests.Attached Files
Supplemental Material - nchembio783-S1.pdf
Supplemental Material - nchembio783-S2.pdf
Supplemental Material - nchembio783-S3.pdf
Supplemental Material - nchembio783-S4.pdf
Supplemental Material - nchembio783-S5.pdf
Supplemental Material - nchembio783-S6.pdf
Supplemental Material - nchembio783-S7.pdf
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Additional details
- Eprint ID
- 87373
- DOI
- 10.1038/nchembio783
- Resolver ID
- CaltechAUTHORS:20180627-083255769
- European Molecular Biology Organization (EMBO)
- Medical Research Council (UK)
- Trinity College
- Overseas Research Studentship Award
- Created
-
2018-06-27Created from EPrint's datestamp field
- Updated
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2021-11-15Created from EPrint's last_modified field