Evidence map›Paper›PMID 42054108›Full record

ArticleChembiochem : a European journal of chemical biology2026

Monoclonal Antibodies Accessing the Cytosol of Living Cells and Binding to Polo-Like Kinase 1 Interdomain Linker Affect Mitotic Behavior.

Clément Steyer, Jean-Christophe Amé, Mariel Donzeau, Karie Shen, Manuela Chiper, Guy Zuber

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Clément SteyerUMR 7242, Biotechnology and Cell Signaling, Université de Strasbourg CNRS, Illkirch, France.
Jean-Christophe AméUMR 7242, Biotechnology and Cell Signaling, Université de Strasbourg CNRS, Illkirch, France.
Mariel DonzeauUMR 7242, Biotechnology and Cell Signaling, Université de Strasbourg CNRS, Illkirch, France.ORCID https://orcid.org/0000-0002-1145-9218
Karie ShenUMR 7242, Biotechnology and Cell Signaling, Université de Strasbourg CNRS, Illkirch, France.
Manuela ChiperUMR 7242, Biotechnology and Cell Signaling, Université de Strasbourg CNRS, Illkirch, France.ORCID https://orcid.org/0000-0002-1563-5397
Guy ZuberUMR 7242, Biotechnology and Cell Signaling, Université de Strasbourg CNRS, Illkirch, France.ORCID https://orcid.org/0000-0001-8032-2410

Funding

Agence Nationale de la Recherche ANR-10-IDEX-0002Agence Nationale de la Recherche ANR-SFRI-0012
6 · The paper itself

Abstract

Polo-like kinase 1 (PLK1) is a master regulator of mitosis and a well-established driver of cancer progression. Strategies to target PLK1 have largely focused on RNA interference using small interfering RNAs or small-molecule inhibitors. Here, we introduce the direct intracellular targeting of the PLK1 interdomain linking the polo-box domain to the kinase domain using monoclonal antibodies. Three monoclonal antibodies recognizing the interdomain region were delivered into the cytosol of HeLa cells by electroporation. These antibodies were shown to bind PLK1 in living cells and to modulate mechanisms involved in mitotic progression. Our results establish these antibodies as tools to probe PLK1 function through real-time labeling and interference with the mitotic machinery.

Indexed as

Antibodies, MonoclonalCell Cycle ProteinsCytosolMitosisProtein Serine-Threonine KinasesProto-Oncogene ProteinsHeLa CellsHumansPolo-Like Kinase 1Protein DomainsAntibodies, MonoclonalCell Cycle ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteinscytosolic deliveryelectroporationmonoclonal antibodiespolo-like kinase 1

Identifiers

PMID42054108
PMCPMC13127698

What OpenQuestion holds

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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.