Evidence map›Paper›PMID 33500394›Full record

ArticleNature communications2021

Orthogonal translation enables heterologous ribosome engineering in E. coli.

Natalie S Kolber, Ranan Fattal, Sinisa Bratulic, Gavriela D Carver, Ahmed H Badran

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

16 citing papers in PubMed, 38 citations in OpenAlex.

  1. Ribosome engineering enhances genetic code expansion inSynthetic and systems biotechnology · 2027
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  8. Autonomous ribosome biogenesis in vitro.Nature communications · 2025
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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

5 authors at 1 institution in 2 countries.

Natalie S KolberBroad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID http://orcid.org/0000-0003-4498-9431
Ranan FattalBroad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.
Sinisa BratulicBroad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID http://orcid.org/0000-0002-1663-2227
Gavriela D CarverBroad Institute of MIT and Harvard, Cambridge, MA, 02142, USA.ORCID http://orcid.org/0000-0001-9371-4157
Ahmed H BadranBroad Institute of MIT and Harvard, Cambridge, MA, 02142, USA. ahbadran@broadinstitute.org.ORCID http://orcid.org/0000-0002-8105-1883
Broad Institute · US

Funding

Functional Interrogation Of Ribosomal Biology Using Continuous EvolutionDP5OD024590 · OD · SCRIPPS RESEARCH INSTITUTE, THE · PI BADRAN, AHMED HUSSEIN · 2017 to 2021
$2.2M
NIH HHS DP5 OD024590
6 · The paper itself

Abstract

The ribosome represents a promising avenue for synthetic biology, but its complexity and essentiality have hindered significant engineering efforts. Heterologous ribosomes, comprising rRNAs and r-proteins derived from different microorganisms, may offer opportunities for novel translational functions. Such heterologous ribosomes have previously been evaluated in E. coli via complementation of a genomic ribosome deficiency, but this method fails to guide the engineering of refractory ribosomes. Here, we implement orthogonal ribosome binding site (RBS):antiRBS pairs, in which engineered ribosomes are directed to researcher-defined transcripts, to inform requirements for heterologous ribosome functionality. We discover that optimized rRNA processing and supplementation with cognate r-proteins enhances heterologous ribosome function for rRNAs derived from organisms with ≥76.1% 16S rRNA identity to E. coli. Additionally, some heterologous ribosomes undergo reduced subunit exchange with E. coli-derived subunits. Cumulatively, this work provides a general framework for heterologous ribosome engineering in living cells.

Indexed as

Bacterial ProteinsEscherichia coliPhylogenyProtein BiosynthesisRibosomal ProteinsRibosomesRNA, BacterialRNA, Ribosomal, 16SRNA, Ribosomal, 23SrRNA OperonSynthetic BiologyBacterial ProteinsRibosomal ProteinsRNA, BacterialRNA, Ribosomal, 16SRNA, Ribosomal, 23S

Identifiers

PMID33500394
PMCPMC7838251
OpenAlexW3121145376

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.