Evidence map›Paper›PMID 33273552›Full record

ArticleScientific reports2020

Algorithms for ribosome traffic engineering and their potential in improving host cells' titer and growth rate.

Hadas Zur, Rachel Cohen-Kupiec, Sophie Vinokour, Tamir Tuller

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Negative feedback and oscillations in a model for mRNA translation.Journal of the Royal Society, Interface · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. On the gain of entrainment in theJournal of the Royal Society, Interface · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Determinants of efficient modulation of ribosomal traffic jams.Computational and structural biotechnology journal · 2021
    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.

Hadas ZurDepartment of Biomedical Engineering, the Engineering Faculty, Tel Aviv University, Tel-Aviv, Israel.
Rachel Cohen-KupiecDepartment of Biomedical Engineering, the Engineering Faculty, Tel Aviv University, Tel-Aviv, Israel.
Sophie VinokourDepartment of Biomedical Engineering, the Engineering Faculty, Tel Aviv University, Tel-Aviv, Israel.
Tamir TullerDepartment of Biomedical Engineering, the Engineering Faculty, Tel Aviv University, Tel-Aviv, Israel. tamirtul@post.tau.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

mRNA translation is a fundamental cellular process consuming most of the intracellular energy; thus, it is under extensive evolutionary selection for optimization, and its efficiency can affect the host's growth rate. We describe a generic approach for improving the growth rate (fitness) of any organism by introducing synonymous mutations based on comprehensive computational models. The algorithms introduce silent mutations that may improve the allocation of ribosomes in the cells via the decreasing of their traffic jams during translation respectively. As a result, resources availability in the cell changes leading to improved growth-rate. We demonstrate experimentally the implementation of the method on Saccharomyces cerevisiae: we show that by introducing a few mutations in two computationally selected genes the mutant's titer increased. Our approach can be employed for improving the growth rate of any organism providing the existence of data for inferring models, and with the relevant genomic engineering tools; thus, it is expected to be extremely useful in biotechnology, medicine, and agriculture.

Indexed as

AlgorithmsCodonComputational BiologyEscherichia coliEscherichia coli ProteinsMutationProtein BiosynthesisRibosomesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCodonEscherichia coli ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID33273552
PMCPMC7713304

What OpenQuestion holds

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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.