Evidence map›Paper›PMID 32251274›Full record

ArticleNature communications2020

An expanded library of orthogonal split inteins enables modular multi-peptide assemblies.

Filipe Pinto, Ella Lucille Thornton, Baojun Wang

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 93 citations in OpenAlex.

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  8. Programming Next-Generation Synthetic Biosensors by Genetic Circuit Design.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  11. Gene Therapy for Inherited Cardiac Arrhythmias.Journal of cardiovascular translational research · 2025
    Review
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  15. Why cellular computations challenge our design principles.Seminars in cell & developmental biology · 2025
    Review
  16. Review
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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

3 authors at 1 institution in 1 country.

Filipe PintoSchool of Biological Sciences, University of Edinburgh, Edinburgh, EH9 3FF, UK.ORCID http://orcid.org/0000-0002-8554-6648
Ella Lucille ThorntonSchool of Biological Sciences, University of Edinburgh, Edinburgh, EH9 3FF, UK.ORCID http://orcid.org/0000-0001-7599-0561
Baojun WangSchool of Biological Sciences, University of Edinburgh, Edinburgh, EH9 3FF, UK. baojun.wang@ed.ac.uk.ORCID http://orcid.org/0000-0002-4858-8937
University of Edinburgh · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N007212/1Medical Research Council MR/S018875/1
6 · The paper itself

Abstract

Inteins are protein segments capable of joining adjacent residues via a peptide bond. In this process known as protein splicing, the intein itself is not present in the final sequence, thus achieving scarless peptide ligation. Here, we assess the splicing activity of 34 inteins (both uncharacterized and known) using a rapid split fluorescent reporter characterization platform, and establish a library of 15 mutually orthogonal split inteins for in vivo applications, 10 of which can be simultaneously used in vitro. We show that orthogonal split inteins can be coupled to multiple split transcription factors to implement complex logic circuits in living organisms, and that they can also be used for the in vitro seamless assembly of large repetitive proteins with biotechnological relevance. Our work demonstrates the versatility and vast potential of an expanded library of orthogonal split inteins for their use in the fields of synthetic biology and protein engineering.

Indexed as

Gene LibraryProtein SplicingBiotechnologyCloning, MolecularFeasibility StudiesFluorescenceGenes, ReporterInteinsLuminescent ProteinsPeptidesPlasmidsProtein EngineeringRecombinant Fusion ProteinsRed Fluorescent ProteinTranscription FactorsTransformation, BacterialLuminescent ProteinsPeptidesRecombinant Fusion ProteinsRed Fluorescent ProteinTranscription Factors

Identifiers

PMID32251274
PMCPMC7090010
OpenAlexW3012782981

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.