Evidence map›Paper›PMID 25232050›Full record

ArticleJournal of the Royal Society, Interface2014

Maximizing protein translation rate in the non-homogeneous ribosome flow model: a convex optimization approach.

Gilad Poker, Yoram Zarai, Michael Margaliot, Tamir Tuller

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. On the gain of entrainment in theJournal of the Royal Society, Interface · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Determinants of efficient modulation of ribosomal traffic jams.Computational and structural biotechnology journal · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Entrainment in the master equation.Royal Society open science · 2018
    Article
  12. Article
  13. Ribosome flow model with extended objects.Journal of the Royal Society, Interface · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. A model for competition for ribosomes in the cell.Journal of the Royal Society, Interface · 2016
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Gilad PokerSchool of EE-Systems, Tel Aviv University, Tel Aviv 69978, Israel.
Yoram ZaraiSchool of EE-Systems, Tel Aviv University, Tel Aviv 69978, Israel.
Michael MargaliotSchool of EE-Systems, Tel Aviv University, Tel Aviv 69978, Israel The Sagol School of Neuroscience, Tel Aviv University, Tel Aviv 69978, Israel.
Tamir TullerThe Sagol School of Neuroscience, Tel Aviv University, Tel Aviv 69978, Israel Department of Biomedical Engineering, Tel Aviv University, Tel Aviv 69978, Israel tamirtul@post.tau.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Translation is an important stage in gene expression. During this stage, macro-molecules called ribosomes travel along the mRNA strand linking amino acids together in a specific order to create a functioning protein. An important question, related to many biomedical disciplines, is how to maximize protein production. Indeed, translation is known to be one of the most energy-consuming processes in the cell, and it is natural to assume that evolution shaped this process so that it maximizes the protein production rate. If this is indeed so then one can estimate various parameters of the translation machinery by solving an appropriate mathematical optimization problem. The same problem also arises in the context of synthetic biology, namely, re-engineer heterologous genes in order to maximize their translation rate in a host organism. We consider the problem of maximizing the protein production rate using a computational model for translation-elongation called the ribosome flow model (RFM). This model describes the flow of the ribosomes along an mRNA chain of length n using a set of n first-order nonlinear ordinary differential equations. It also includes n + 1 positive parameters: the ribosomal initiation rate into the mRNA chain, and n elongation rates along the chain sites. We show that the steady-state translation rate in the RFM is a strictly concave function of its parameters. This means that the problem of maximizing the translation rate under a suitable constraint always admits a unique solution, and that this solution can be determined using highly efficient algorithms for solving convex optimization problems even for large values of n. Furthermore, our analysis shows that the optimal translation rate can be computed based only on the optimal initiation rate and the elongation rate of the codons near the beginning of the ORF. We discuss some applications of the theoretical results to synthetic biology, molecular evolution, and functional genomics.

Indexed as

AlgorithmsComputer SimulationModels, BiologicalCodonOpen Reading FramesPeptide Chain Elongation, TranslationalRibosomesCodonconcavitygene translationmaximizing the protein production ratesynthetic biologytranscript evolution

Identifiers

PMID25232050
PMCPMC4191103

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.