Evidence map›Paper›PMID 42156793›Full record

ArticleScientific reports2026

Human cathelicidin peptide LL-37 compacts nucleic acids and alters neutrophil extracellular trap structure.

Claudia Zielke, Behzad Rad, Josefine E Nielsen, Jiaxin Li, Sopida Pimcharoen, Manasi Sawant, Seraphine Kamayirese, Jennifer S Lin, Hawa R Thiam, Annelise E Barron

Abstract read
In one paragraph

Article in Scientific reports, 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

10 authors.

Claudia ZielkeDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Behzad RadMolecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, USA.
Josefine E NielsenDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Jiaxin LiDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Sopida PimcharoenDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Manasi SawantDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Seraphine KamayireseDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Jennifer S LinDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Hawa R ThiamDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA.
Annelise E BarronDepartment of Bioengineering, Schools of Medicine and of Engineering, Stanford University, Stanford, CA, 94305, USA. aebarron@stanford.edu.

Funding

NIH HHS DP1 OD029517Novo Nordisk Fonden NNF21OC0068675
6 · The paper itself

Abstract

The human cathelicidin host defense peptide LL-37 is expressed by many cell types, including neutrophils, macrophages, and epithelial cells, and forms complexes with nucleic acids that can have either beneficial or detrimental health effects. We suggest that these differential impacts are directly connected to the extent of nucleic acid binding by LL-37. Here, we use phage λ DNA and techniques such as high-resolution video microscopy, gel electrophoresis, circular dichroism, and displacement assays to show that LL-37 binds non-specifically to dsDNA, condensing it, followed by formation of progressively larger complexes from smaller domains, until "complete" complexation is attained at a (w/w) ratio of DNA/LL-37 of 1:1.7. The morphology of these complexes is concentration-dependent, with relatively low LL-37 amounts yielding loosely aggregated DNA structures and higher LL-37 concentrations leading to well-defined, disc-like complexes of about 150 nm in diameter. The condensation of nucleic acids, which causes a loss of the characteristic B-DNA features, results from interactions of the phosphodiester backbone with cationic amino acid side chains of the peptide at physiological pH, most likely in A-T rich sequences of the nucleic acid. Our results show that the α-helical structure of the peptide with its amphipathic and hydrophobic surfaces is essential. Finally, we show that LL-37 complexation alters the structure of neutrophil extracellular traps (NETs), causing a significant reduction in projected NET area at high LL-37 concentrations. Our data suggest that LL-37 helps prevent nucleic acid dispersal and condenses dsDNA, which may impact the biophysics of NET clearance.

Indexed as

Antimicrobial Cationic PeptidesDNAExtracellular TrapsNeutrophilsBacteriophage lambdaCathelicidinsHumansNucleic Acid ConformationProtein BindingAntimicrobial Cationic PeptidesCathelicidinsDNAAntimicrobial peptideCondensationInnate immunityIntermolecular interactionsLambda DNALL-37

Identifiers

PMID42156793
PMCPMC13379582

What OpenQuestion holds

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Registered trials

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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.