Evidence map›Paper›PMID 36810740›Full record

ArticleNature communications2023

Community science designed ribosomes with beneficial phenotypes.

Antje Krüger, Andrew M Watkins, Roger Wellington-Oguri, Jonathan Romano, Camila Kofman, Alysse DeFoe, Yejun Kim, Jeff Anderson-Lee, Eli Fisker, Jill Townley and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Computational De Novo Design of Group II Introns Yields Highly Active Ribozymes.Chembiochem : a European journal of chemical biology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Cell-free Biosynthesis of Peptidomimetics.Biotechnology and bioprocess engineering : BBE · 2023
    Review
  8. Article
  9. 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

14 authors.

Antje Krüger *Department of Chemical and Biological Engineering, Chemistry of Life Processes Institute, and Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA.ORCID 0000-0002-8155-0682
Andrew M Watkins *Department of Biochemistry, Stanford University, Stanford, CA, 94305, USA.
Roger Wellington-OguriEterna Massive Open Laboratory, Stanford, CA, 94305, USA.
Jonathan RomanoDepartment of Biochemistry, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0003-4031-0102
Camila KofmanDepartment of Chemical and Biological Engineering, Chemistry of Life Processes Institute, and Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA.
Alysse DeFoeDepartment of Chemical and Biological Engineering, Chemistry of Life Processes Institute, and Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA.
Yejun KimDepartment of Chemical and Biological Engineering, Chemistry of Life Processes Institute, and Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA.
Jeff Anderson-LeeEterna Massive Open Laboratory, Stanford, CA, 94305, USA.ORCID 0000-0001-9382-4743
Eli FiskerEterna Massive Open Laboratory, Stanford, CA, 94305, USA.
Jill TownleyEterna Massive Open Laboratory, Stanford, CA, 94305, USA.ORCID 0000-0001-8528-2227
Eterna Participants
Anne E d'AquinoDepartment of Chemical and Biological Engineering, Chemistry of Life Processes Institute, and Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA.
Rhiju DasDepartment of Biochemistry, Stanford University, Stanford, CA, 94305, USA. rhiju@stanford.edu.ORCID 0000-0001-7497-0972
Michael C JewettDepartment of Chemical and Biological Engineering, Chemistry of Life Processes Institute, and Center for Synthetic Biology, Northwestern University, Evanston, IL, 60208, USA. m-jewett@northwestern.edu.ORCID 0000-0003-2948-6211

Funding

Next-generation computational/chemical methods for complex RNA structuresR35GM122579 · NIGMS · STANFORD UNIVERSITY · PI Rhiju Das · 2017 to 2026
$7.2M
NIGMS NIH HHS R35 GM122579
6 · The paper itself

Abstract

Functional design of ribosomes with mutant ribosomal RNA (rRNA) can expand opportunities for understanding molecular translation, building cells from the bottom-up, and engineering ribosomes with altered capabilities. However, such efforts are hampered by cell viability constraints, an enormous combinatorial sequence space, and limitations on large-scale, 3D design of RNA structures and functions. To address these challenges, we develop an integrated community science and experimental screening approach for rational design of ribosomes. This approach couples Eterna, an online video game that crowdsources RNA sequence design to community scientists in the form of puzzles, with in vitro ribosome synthesis, assembly, and translation in multiple design-build-test-learn cycles. We apply our framework to discover mutant rRNA sequences that improve protein synthesis in vitro and cell growth in vivo, relative to wild type ribosomes, under diverse environmental conditions. This work provides insights into rRNA sequence-function relationships and has implications for synthetic biology.

Indexed as

RibosomesRNA, RibosomalPhenotypeRibosomal ProteinsSynthetic BiologyRibosomal ProteinsRNA, Ribosomal

Identifiers

PMID36810740
PMCPMC9944925

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LicenceCC BY
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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.