Evidence map›Paper›PMID 41835586›Full record

ArticleACS omega2026

A Fluorescent Protein-Tagged Scorpion Toxin with Picomolar Affinity for the Kv1.3 K

Jesús Borrego, Muhammad Umair Naseem, Amna Al Olaimi, Eva Korpos, Arpad Szoor, Gyula Batta, Gyorgy Panyi

Abstract read
In one paragraph

Article in ACS omega, 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

7 authors.

Jesús BorregoDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0000-0002-2783-8044
Muhammad Umair NaseemDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0000-0003-3849-6219
Amna Al OlaimiDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0009-0007-5946-8934
Eva KorposDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0000-0002-0438-4211
Arpad SzoorDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0000-0002-3727-6129
Gyula BattaDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0000-0001-8735-6920
Gyorgy PanyiDepartment of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, 1. Egyetem Ter, Debrecen H-4032, Hungary.ORCID https://orcid.org/0000-0001-6227-3301

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fusion of fluorophores and peptide pore blockers generates valuable molecular tools to identify cells that express the voltage-gated potassium channel Kv1.3. Changes in the Kv1.3 expression are associated with numerous autoimmune and neurological disorders. In this study, Vm24, a potent and selective Kv1.3 inhibitor peptide isolated from scorpion venom, was genetically linked to mCherry, a red fluorescent protein characterized by high photostability, maturation, and tagging tolerance. The recombinant fusion protein (mCherry-Vm24) was expressed utilizing the

Identifiers

PMID41835586
PMCPMC12980169

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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.