Evidence map›Paper›PMID 28722655›Full record

ArticleeLife2017

Key steps in unconventional secretion of fibroblast growth factor 2 reconstituted with purified components.

Julia P Steringer, Sascha Lange, Sabína Čujová, Radek Šachl, Chetan Poojari, Fabio Lolicato, Oliver Beutel, Hans-Michael Müller, Sebastian Unger, Ünal Coskun and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.4field-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

44 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
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  7. Article
  8. Endocytic tethers modulate unconventional GAPDH secretion.Cell surface (Amsterdam, Netherlands) · 2025
    Article
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  15. Article
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  17. Silencing a Chitinase Gene,International journal of molecular sciences · 2023
    Article
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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

15 authors at 6 institutions in 4 countries.

Julia P SteringerHeidelberg University Biochemistry Center, Heidelberg, Germany.ORCID 0000-0001-9418-2762
Sascha LangeInstitut für Chemie und Biochemie, Freie Universität Berlin, Berlin, Germany.
Sabína ČujováJ. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Radek ŠachlJ. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Chetan PoojariDepartment of Physics, University of Helsinki, Helsinki, Finland.ORCID 0000-0001-6575-221X
Fabio LolicatoDepartment of Physics, University of Helsinki, Helsinki, Finland.ORCID 0000-0001-7537-0549
Oliver BeutelMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Hans-Michael MüllerHeidelberg University Biochemistry Center, Heidelberg, Germany.
Sebastian UngerHeidelberg University Biochemistry Center, Heidelberg, Germany.ORCID 0000-0003-2525-8502
Ünal CoskunPaul Langerhans Institute Dresden, Helmholtz Zentrum München, University Hospital and Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.ORCID 0000-0003-4375-3144
Alf HonigmannMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Ilpo VattulainenDepartment of Physics, University of Helsinki, Helsinki, Finland.ORCID 0000-0001-7408-3214
Martin HofJ. Heyrovský Institute of Physical Chemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Christian FreundInstitut für Chemie und Biochemie, Freie Universität Berlin, Berlin, Germany.
Walter NickelHeidelberg University Biochemistry Center, Heidelberg, Germany.ORCID 0000-0002-6496-8286
Heidelberg University · DECzech Academy of Sciences, J. Heyrovský Institute of Physical Chemistry · CZUniversity of Helsinki · FIFreie Universität Berlin · DEMax Planck Institute of Molecular Cell Biology and Genetics · DEGerman Center for Diabetes Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FGF2 is secreted from cells by an unconventional secretory pathway. This process is mediated by direct translocation across the plasma membrane. Here, we define the minimal molecular machinery required for FGF2 membrane translocation in a fully reconstituted inside-out vesicle system. FGF2 membrane translocation is thermodynamically driven by PI(4,5)P

Indexed as

Protein MultimerizationFibroblast Growth Factor 2Heparan SulfateMembrane Transport ProteinsMolecular Dynamics SimulationPhosphatidylinositol 4,5-DiphosphateSecretory VesiclesFibroblast Growth Factor 2Heparan SulfateMembrane Transport ProteinsPhosphatidylinositol 4,5-DiphosphatebiochemistrybiophysicsFibroblast Growth Factor 2humanoligomerizationphosphoinositideprotein translocation across membranesreconstitution with purified componentsstructural biologyUnconventional protein secretion

Identifiers

PMID28722655
PMCPMC5601999
OpenAlexW2737451970

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.