Elongation factor P (EF-P) plays a critical role in protein synthesis in bacteria. Loss of EF- P leads to a variety of phenotypes, including metabolic stress, altered antibiotic resistance, and loss of virulence. Although EF-P was discovered in the 1970's, the first compelling explanation of its biological significance appeared in early 2013. Protein synthesis pauses when three or more consecutive prolines occur in the nascent peptide;EF-P binds to the ribosome and restores rapid peptide synthesis. Our goal is to achieve a molecular-level understanding of how polyproline motifs pause translation and how pauses are resolved by EF-P. These studies will shed light on how the nascent peptide modulates translational rates, a phenomenon with important implications for protein folding and gene regulation. The molecular mechanism of pausing is poorly understood. We hypothesize that Pro alters the geometry of key nucleotides in the ribosomal active site, inhibiting catalysis.
In Aim 1 we will test this hypothesis using pre- steady state kinetic methods to isolate rate defects that lead to pausing. We will probe the interaction of the peptide and active site using amino acid analogs and rRNA mutations. We will also investigate how EF-P alleviates ribosome pausing. EF-P has a tRNA-like structure and interacts with peptidyl-tRNA within the ribosome. The Lys34 side chain, positioned near the peptidyl-transferase center, is covalently modified with a ?-lysyl moiety that is essential for EF- P function in E. coli. We hypothesize that the modified side chain subtly rearranges the geometry of the ribosomal active site to restore catalysis.
In Aim 2, we will test the role of the ?-lysyl moiety by chemically modifying EF-P with a series of ?-lysine analogs. Notably, the enzymes responsible for ?-lysylation, YjeA and YjeK, are lacking in 70% of bacteria. We will determine how EF-P is modified in two of these species and identify the enzymes responsible. Finally, our biochemical data suggest that EF-P alleviates translational pausing at several motifs, not just polyproline stretches.
In Aim 3, we will define the scope of EF-P activity using ribosome profiling, a method for monitoring translation globally in living cell. By monitoring changes in translation and mRNA expression, we will link pausing to the pleiotropic phenotypes observed in cells lacking EF-P.

Public Health Relevance

These studies will increase our understanding of how bacterial ribosomes synthesize proteins. They will shed light on why ribosomes pause during translation and how paused ribosomes are restarted for protein synthesis to continue. This mechanistic insight may be useful in designing antibiotics that target bacterial ribosomes.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
Research Project (R01)
Project #
Application #
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Bender, Michael T
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Johns Hopkins University
Schools of Medicine
United States
Zip Code
Schuller, Anthony P; Wu, Colin Chih-Chien; Dever, Thomas E et al. (2017) eIF5A Functions Globally in Translation Elongation and Termination. Mol Cell 66:194-205.e5
Hwang, Jae-Yeon; Buskirk, Allen R (2017) A ribosome profiling study of mRNA cleavage by the endonuclease RelE. Nucleic Acids Res 45:327-336
Buskirk, Allen R; Green, Rachel (2017) Ribosome pausing, arrest and rescue in bacteria and eukaryotes. Philos Trans R Soc Lond B Biol Sci 372:
Mohammad, Fuad; Woolstenhulme, Christopher J; Green, Rachel et al. (2016) Clarifying the Translational Pausing Landscape in Bacteria by Ribosome Profiling. Cell Rep 14:686-694
Woolstenhulme, Christopher J; Guydosh, Nicholas R; Green, Rachel et al. (2015) High-precision analysis of translational pausing by ribosome profiling in bacteria lacking EFP. Cell Rep 11:13-21
Starosta, Agata L; Lassak, J├╝rgen; Peil, Lauri et al. (2014) A conserved proline triplet in Val-tRNA synthetase and the origin of elongation factor P. Cell Rep 9:476-83
Miller, Mickey R; Buskirk, Allen R (2014) The SmpB C-terminal tail helps tmRNA to recognize and enter stalled ribosomes. Front Microbiol 5:462