Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Sep 17;123(18):3010-3023.
doi: 10.1016/j.bpj.2024.05.032. Epub 2024 Jun 6.

On the response of elongating ribosomes to forces opposing translocation

Affiliations

On the response of elongating ribosomes to forces opposing translocation

Peter B Moore. Biophys J. .

Abstract

The elongation phase of protein synthesis is a cyclic, steady-state process. It follows that its directionality is determined by the thermodynamics of the accompanying chemical reactions, which strongly favor elongation. Its irreversibility is guaranteed by its coupling to those reactions, rather being a consequence of any of the conformational changes that occur as it unfolds. It also follows that, in general, the rate of elongation is not proportional to the forward rate constants of any of its steps, including its final, mechano-chemical step, translocation. Instead, the reciprocal of the rate of elongation should be linearly related to the reciprocal of those rate constants. When the results of experiments done a decade ago to measure the effect that forces opposing translocation have on the rate of elongation are reinterpreted in light of these findings, it becomes clear that translocation was rate limiting under conditions in which those experiments were done, and that it is likely to be a Brownian ratchet process, as was concluded earlier.

PubMed Disclaimer

Conflict of interest statement

Declaration of interests The authors declare no competing interests.

Comment in

  • Taming the ribosome.
    Puglisi JD. Puglisi JD. Biophys J. 2024 Sep 17;123(18):2964-2965. doi: 10.1016/j.bpj.2024.07.045. Epub 2024 Aug 2. Biophys J. 2024. PMID: 39097772 No abstract available.

Similar articles

Cited by

  • Taming the ribosome.
    Puglisi JD. Puglisi JD. Biophys J. 2024 Sep 17;123(18):2964-2965. doi: 10.1016/j.bpj.2024.07.045. Epub 2024 Aug 2. Biophys J. 2024. PMID: 39097772 No abstract available.

References

    1. Jobe A., Liu Z., et al. Frank J. New Insights into Ribosome Structure and Function. Cold Spring Harbor Perspect. Biol. 2019;11:a032615. doi: 10.1101/cshperspect.a032615. - DOI - PMC - PubMed
    1. Rodnina M.V., Wintermeyer W. Protein Elongation, Co-translational Folding and Targeting. J. Mol. Biol. 2016;428:2165–2185. doi: 10.1016/j.jmb.2016.03.22. - DOI - PubMed
    1. Voorhees R.M., Ramakrishnan V. Structural basis of the translational elongation cycle. Annu. Rev. Biochem. 2013;82:203–236. doi: 10.1146/annurev-biochem-113009-092313. - DOI - PubMed
    1. Rudorf S., Thommen M., et al. Lipowsky R. Deducing the kinetics of protein synthesis in vivo from the transition rates measured in vitro. PLoS Comput. Biol. 2014;10 doi: 10.1371/journal.pcbi.1003909. - DOI - PMC - PubMed
    1. Rudorf S., Lipowsky R. Protein synthesis in E. coli: dependence of codon-specific elongation on tRNA concentration and codon usage. PLoS One. 2015;10 doi: 10.1371/journal.pone.0134994. - DOI - PMC - PubMed

LinkOut - more resources