Evidence map›Paper›PMID 31748551›Full record

ArticleNature communications2019

Towards the application of Tc toxins as a universal protein translocation system.

Daniel Roderer, Evelyn Schubert, Oleg Sitsel, Stefan Raunser

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Review
  6. Evaluating TcAs for Use in Biotechnology Applications.Biotech (Basel (Switzerland)) · 2025
    Article
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  8. 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

4 authors at 1 institution in 1 country.

Daniel RodererDepartment of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Otto-Hahn-Str. 11, 44227, Dortmund, Germany.ORCID https://orcid.org/0000-0002-7276-3467
Evelyn SchubertDepartment of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Otto-Hahn-Str. 11, 44227, Dortmund, Germany.ORCID https://orcid.org/0000-0003-2625-1505
Oleg SitselDepartment of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Otto-Hahn-Str. 11, 44227, Dortmund, Germany.ORCID http://orcid.org/0000-0002-4496-7489
Stefan RaunserDepartment of Structural Biochemistry, Max Planck Institute of Molecular Physiology, Otto-Hahn-Str. 11, 44227, Dortmund, Germany. stefan.raunser@mpi-dortmund.mpg.de.ORCID https://orcid.org/0000-0001-9373-3016
Max Planck Institute of Molecular Physiology · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tc toxins are bacterial protein complexes that inject cytotoxic enzymes into target cells using a syringe-like mechanism. Tc toxins are composed of a membrane translocator and a cocoon that encapsulates a toxic enzyme. The toxic enzyme varies between Tc toxins from different species and is not conserved. Here, we investigate whether the toxic enzyme can be replaced by other small proteins of different origin and properties, namely Cdc42, herpes simplex virus ICP47, Arabidopsis thaliana iLOV, Escherichia coli DHFR, Ras-binding domain of CRAF kinase, and TEV protease. Using a combination of electron microscopy, X-ray crystallography and in vitro translocation assays, we demonstrate that it is possible to turn Tc toxins into customizable molecular syringes for delivering proteins of interest across membranes. We also infer the guidelines that protein cargos must obey in terms of size, charge, and fold in order to apply Tc toxins as a universal protein translocation system.

Indexed as

Arabidopsis ProteinsBacterial ProteinsBacterial Toxinscdc42 GTP-Binding ProteinCrystallography, X-RayEndopeptidasesEscherichia coli ProteinsImmediate-Early ProteinsMicroscopy, ElectronModels, MolecularPhotorhabdusProtein Translocation SystemsProto-Oncogene Proteins c-rafTetrahydrofolate DehydrogenaseArabidopsis ProteinsBacterial ProteinsBacterial Toxinscdc42 GTP-Binding ProteinEndopeptidasesEscherichia coli ProteinsICP47 protein, Herpes simplex virusImmediate-Early ProteinsProtein Translocation SystemsProto-Oncogene Proteins c-rafTetrahydrofolate DehydrogenaseTEV protease

Identifiers

PMID31748551
PMCPMC6868009
OpenAlexW2991116009

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.