Evidence map›Paper›PMID 42507016›Full record

ArticleEuropean biophysics journal : EBJ2026

Clustering of the T-cell receptor complex may facilitate T-cell activation by stretching of CD3ζ cytoplasmic tails.

Steven Siegl, Sebastian Fürthauer, Gerhard J Schütz

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Article in European biophysics journal : EBJ, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Steven SieglInstitute of Applied Physics, TU Wien, Lehargasse 6, 1060, Vienna, Austria.
Sebastian FürthauerInstitute of Applied Physics, TU Wien, Lehargasse 6, 1060, Vienna, Austria. fuerthauer@iap.tuwien.ac.at.ORCID http://orcid.org/0000-0001-9581-5963
Gerhard J SchützInstitute of Applied Physics, TU Wien, Lehargasse 6, 1060, Vienna, Austria. schuetz@iap.tuwien.ac.at.ORCID http://orcid.org/0000-0003-1542-1089

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivated by experimental observations that T-cells can activate as a consequence of clustering of T-cell receptors, we hypothesize that steric confinement between the intracellular chains of the TCR could play a role. Using coarse-grained simulations, we show that steric interactions between TCRs are sufficient to induce appreciable stretch of the intracellular domains of CD3ζ chains. We propose a model, in which the difference in membrane distances between the phosphatase CD45 and the kinases lck and fyn is able to sense the clustering-induced CD3ζ stretch: we estimate a 1.5- to 2-fold increase in phosphorylation of immunoreceptor tyrosine-based activation motifs (ITAMs) at CD3ζ upon TCR clustering.

Indexed as

Intrinsically disordered proteinsPolymer physicsSignalingT-cell biophysicsT-cell receptorTransmembrane proteins

Identifiers

What OpenQuestion holds

Textmetadata
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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.