Evidence map›Paper›PMID 40181613›Full record

ArticleSmall methods2025

Imaging Ligand-Receptor Interactions at Single-Protein Resolution with DNA-PAINT.

Monique Honsa, Isabelle Pachmayr, Larissa Heinze, Levent Bas, Luciano A Masullo, Jisoo Kwon, Ana Perovic, Brenda Schulman, Ralf Jungmann

Abstract read
In one paragraph

Article in Small methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Quantitative nanoscale imaging shows peptide-MHC I complexes are monomeric and spatially regulated in human dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. 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

9 authors.

Monique HonsaMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.ORCID https://orcid.org/0009-0005-5937-9646
Isabelle PachmayrMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.ORCID https://orcid.org/0000-0002-3422-8340
Larissa HeinzeMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.
Levent BasMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.
Luciano A MasulloMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.ORCID https://orcid.org/0000-0001-8664-5448
Jisoo KwonMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.
Ana PerovicMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.
Brenda SchulmanMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.ORCID https://orcid.org/0000-0002-3083-1126
Ralf JungmannMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Planegg, Germany.ORCID https://orcid.org/0000-0003-4607-3312

Funding

BMBF 13N15990Danish National Research Foundation DNRF135European Research Council 101003275European Union's Horizon 20212022 research and innovation program 101065980International Max Planck Research School for Molecules of Life IMPRS-MLVolkswagen Foundation 98198
6 · The paper itself

Abstract

Ligand-receptor interactions are critical for cell communication, with membrane receptors such as the Epidermal Growth Factor Receptor (EGFR) mediating responses to external signals. Super-resolution microscopy techniques in principle allow the visualization of these interactions at single-molecule resolution. While DNA-Points Accumulation for Imaging in Nanoscale Topography (DNA-PAINT) super-resolution microscopy has been successfully used to image receptors, specific labeling of cognate ligands, such as EGF, with DNA has remained challenging. Here, an approach to label and image the small extracellular ligand EGF using site-specific tagging and DNA modification is presented. Functional, site-specifically tagged EGF constructs, including DNA-conjugated and ALFA-tagged EGF, are generated. When compared to the native ligand, only the ALFA-tagged EGF maintains full functionality such as efficient EGFR clustering and internalization, while the DNA-conjugated EGF exhibits reduced EGFR oligomerization. 3D DNA-PAINT imaging of the ALFA-tagged EGF, when bound to EGFR, reveals spatial arrangements of EGF-EGFR complexes and captures different stages of receptor internalization. The labeling approach enables precise visualization of ligand-receptor interactions at high resolution and, in principle, can be extended to other ligand-receptor systems.

Indexed as

DNAEpidermal Growth FactorErbB ReceptorsSingle Molecule ImagingHumansLigandsProtein BindingDNAEpidermal Growth FactorErbB ReceptorsLigandsDNA‐PAINTEGFRligand‐receptor interactionsmembrane receptorssingle‐molecule imagingsuper‐resolution imaging

Identifiers

PMID40181613
PMCPMC12182887

What Socratic holds

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LicenceCC BY
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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 Socratic graph.