Evidence map›Paper›PMID 42136026›Full record

ArticleBiophysical journal2026

Iomeprol X-ray contrast media alter conformation and affinity of the ATP binding pocket of actin.

Elek Telek, Gábor Hild, Veronika Takács-Kollár, Balázs Zoltán Zsidó, Csaba Hetényi, Kinga Ujfalusi-Pozsonyi, Zétény Csonka, Bálint Bécsi, András Lukács, Sándor Kunsági-Máté and 2 more

Abstract read
In one paragraph

Article in Biophysical journal, 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

12 authors.

Elek TelekDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Gábor HildDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Veronika Takács-KollárDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Balázs Zoltán ZsidóPharmacoinformatics Unit, Department of Pharmacology and Pharmacotherapy, Medical School, University of Pécs, Szigeti str 12, 7624 Pécs, Hungary.
Csaba HetényiPharmacoinformatics Unit, Department of Pharmacology and Pharmacotherapy, Medical School, University of Pécs, Szigeti str 12, 7624 Pécs, Hungary; National Laboratory for Drug Research and Development, Budapest, Hungary.
Kinga Ujfalusi-PozsonyiDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Zétény CsonkaDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Bálint BécsiDepartment of Medical Chemistry, Faculty of Medicine, University of Debrecen, Egyetem square 1, 4043 Debrecen, Hungary.
András LukácsDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Sándor Kunsági-MátéDepartment of Organic and Medicinal Chemistry, Faculty of Pharmacy, University of Pécs, Honvéd str 1, 7624 Pécs, Hungary; János Szentágothai Research Center, Ifjúság útja 20, 7624 Pécs, Hungary.
Gabriella HildLanguages for Biomedical Purposes and Communication, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary.
Zoltán UjfalusiDepartment of Biophysics, Medical School, University of Pécs, Szigeti str. 12, 7624 Pécs, Hungary. Electronic address: zoltan.ujfalusi@aok.pte.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contrast materials are widely used in various X-ray/CT and MRI diagnostic procedures. When administered in high volumes, contrast agents can strain kidney function and lead to acute renal failure. Contrast materials may damage the plasma membrane and penetrate into tissue cells. Some iodine-based contrast agents have been reported to distort the shape of red blood cells, implying a rearrangement of the actin cytoskeletal network. As actin plays a crucial role in numerous cellular processes, the effects of iodine-based contrast media on actin require clarification. We characterized the effect of iomeprol on the structure and function of actin using calorimetry, co-sedimentation, fluorescence spectroscopy, and molecular docking. Our results revealed that iomeprol disassembles the F-actin network by interacting with G-actin, suggesting a direct influence on its structural and functional properties. In line with this, polymerization and dilution-induced depolymerization assays, as well as critical concentration measurements, showed pronounced effects on actin dynamics. Iomeprol alters the conformation of G-actin, particularly the ATP-binding pocket-which becomes more open-and significantly (∼3-fold) decreases ATP affinity. Molecular docking supported these findings, indicating that iomeprol interacts with the ATP-binding cleft of G-actin. An additional interaction site was identified in the SD1/3 cleft-a known binding site for Wiskott-Aldrich syndrome protein and profilin-suggesting that iomeprol may also influence the association and dissociation dynamics of actin-binding proteins. Overall, our findings indicate that iomeprol can influence the structural and functional properties of actin, raising the possibility that such alterations may contribute to changes in actin organization and, consequently, to actin-dependent cellular processes.

Indexed as

ActinsAdenosine TriphosphateContrast MediaAnimalsBinding SitesMolecular Docking SimulationProtein BindingProtein ConformationActinsAdenosine TriphosphateContrast Media

Identifiers

PMID42136026
PMCPMC13507453

What OpenQuestion holds

Textmetadata
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.