Evidence map›Paper›PMID 31320676›Full record

ArticleScientific reports2019

Dynamics and distribution of paxillin, vinculin, zyxin and VASP depend on focal adhesion location and orientation.

Karin Legerstee, Bart Geverts, Johan A Slotman, Adriaan B Houtsmuller

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 104 citations in OpenAlex.

  1. ILK binding to β1 integrin is indirect and mediated by kindlin-2.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  8. Calpain-2-Mediated Endothelial Focal Adhesion Disruption in Thoracic Aortic Dissection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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3 more citing papers are in PubMed but not listed here.

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.

Karin LegersteeErasmus Medical Centre Rotterdam, Department of Pathology, Optical Imaging Centre, Rotterdam, The Netherlands.
Bart GevertsErasmus Medical Centre Rotterdam, Department of Pathology, Optical Imaging Centre, Rotterdam, The Netherlands.
Johan A SlotmanErasmus Medical Centre Rotterdam, Department of Pathology, Optical Imaging Centre, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-9705-9620
Adriaan B HoutsmullerErasmus Medical Centre Rotterdam, Department of Pathology, Optical Imaging Centre, Rotterdam, The Netherlands. a.houtsmuller@erasmusmc.nl.ORCID http://orcid.org/0000-0003-0967-0740
Erasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Focal adhesions (FAs) are multiprotein structures that link the intracellular cytoskeleton to the extracellular matrix. They mediate cell adhesion and migration, crucial to many (patho-) physiological processes. We examined in two cell types from different species the binding dynamics of functionally related FA protein pairs: paxillin and vinculin versus zyxin and VASP. In photobleaching experiments ~40% of paxillin and vinculin remained stably associated with a FA for over half an hour. Zyxin and VASP predominantly displayed more transient interactions. We show protein binding dynamics are influenced by FA location and orientation. In FAs located close to the edge of the adherent membrane paxillin, zyxin and VASP were more dynamic and had larger bound fractions. Zyxin and VASP were also more dynamic and had larger bound fractions at FAs perpendicular compared to parallel to this edge. Finally, we developed a photoconversion assay to specifically visualise stably bound proteins within subcellular structures and organelles. This revealed that while paxillin and vinculin are distributed evenly throughout FAs, their stably bound fractions form small clusters within the FA-complex. These clusters are more concentrated for paxillin than for vinculin and are mostly found at the proximal half of the FA where actin also enters.

Indexed as

AnimalsBone NeoplasmsCell Adhesion MoleculesCytoskeletonDogsExtracellular MatrixFocal AdhesionsHumansMadin Darby Canine Kidney CellsMicrofilament ProteinsOsteosarcomaPaxillinPhosphoproteinsTumor Cells, CulturedVasodilator-Stimulated PhosphoproteinVinculinCell Adhesion MoleculesMicrofilament ProteinsPaxillinPhosphoproteinsPXN protein, humanVasodilator-Stimulated PhosphoproteinVCL protein, humanVinculinZyxinZYX protein, human

Identifiers

PMID31320676
PMCPMC6639384
OpenAlexW2956745804

What OpenQuestion holds

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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.