# Collagen-targeted tracers for molecular imaging of atrial fibrosis and sensitive detection of atrial fibrillation

**Authors:** Be’eri Niego, Christoph E. Hagemeyer, Bianca Jupp, Asif Noor, Paul S. Donnelly, Rong Xu, Thirimadura V. H. Mendis, Yi Ching Chen, Irena Carmichael, Julie R. McMullen, Karen Alt

PMC · DOI: 10.1038/s44325-025-00086-2 · npj Cardiovascular Health · 2025-10-06

## TL;DR

Researchers developed collagen-targeted tracers to detect atrial fibrosis and atrial fibrillation, offering a new way to diagnose and monitor these heart conditions.

## Contribution

The novel T-peptide tracer shows disease stage sensitivity, improving detection of atrial fibrosis and AF.

## Key findings

- Collagen-targeted tracers accumulated in fibrotic atria compared to controls.
- T-peptide showed specific uptake and fast renal clearance in mice.
- Tracers enable earlier detection of atrial fibrosis and associated arrhythmias.

## Abstract

Atrial fibrillation (AF), often accompanied by atrial fibrosis, is challenging to diagnose sub-clinically and reverse once established. Molecular imaging targeting excess atrial collagen may enable earlier detection of atrial fibrosis and its associated arrhythmias. We used the collagen I-binding peptide EP-3533 and our novel ‘T-peptide’ targeting matrix metalloproteinases-2-digested collagen IV to image interstitial atrial fibrosis, AF and heart failure (HF) that develop in the double transgenic mouse model dnPI3K-Mst1 (termed ‘AF + HF’). Ex vivo and in vivo imaging were performed using near-infrared scans and positron emission tomography (PET) with probes conjugated to Cyanine5.5 and copper-64, respectively. Both tracers significantly accumulated in fibrotic atria compared to non-transgenic controls, with specific T-peptide uptake relative to a mutated ‘S-peptide’. Pharmacokinetic profiling demonstrated good tracer plasma stability and fast renal clearance. These results highlight the potential of collagen-targeted peptide tracers, particularly the disease stage-sensitive T-peptide, to improve diagnosis and monitoring of atrial fibrosis and AF.

## Linked entities

- **Proteins:** vkg (viking)
- **Chemicals:** T-peptide (PubChem CID 138991781), copper-64 (PubChem CID 105141), S-peptide (PubChem CID 16197277)
- **Diseases:** atrial fibrillation (MONDO:0004981), heart failure (MONDO:0005252)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Adrb2 (adrenergic receptor, beta 2) [NCBI Gene 11555] {aka Adrb-2, Badm, Gpcr7}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, St3gal5 (ST3 beta-galactoside alpha-2,3-sialyltransferase 5) [NCBI Gene 20454] {aka 3S-T, Siat9, [a]2}, Mmp2 (matrix metallopeptidase 2) [NCBI Gene 17390] {aka Clg4a, GelA, MMP-2}, Stk4 (serine/threonine kinase 4) [NCBI Gene 58231] {aka Kas-2, Mst1, Ysk3}, Mst1 (macrophage stimulating 1 (hepatocyte growth factor-like)) [NCBI Gene 15235] {aka D3F15S2h, D9H3F15S2, DNF15S2h, Hgfl}
- **Diseases:** tumor (MESH:D009369), cardiac arrest (MESH:D006323), atrial and ventricular fibrosis (MESH:D005355), cardiac inflammation (MESH:D007249), atrial disease (MESH:D004194), Cardiac arrhythmias (MESH:D001145), left ventricular (LV) fibrosis (MESH:D018487), stroke (MESH:D020521), cardiomyopathies (MESH:D009202), AF (MESH:D001281), cardiovascular conditions (MESH:D002318), DCM (MESH:D002311), MI (MESH:D009203), toxicity (MESH:D064420), fibrotic abnormalities (MESH:D000014), atrial thrombosis (MESH:D013927), cardio-inflammatory (MESH:D059347), atrial flutter (MESH:D001282), supraventricular tachycardia (MESH:D013617), ventricular disease (MESH:D014693), overdose (MESH:D062787), HF (MESH:D006333), cardiac (MESH:D006331), pulmonary fibrosis (MESH:D011658), hypertrophic (MESH:D002312), atrial myopathy (MESH:D009135), atrial enlargement (MESH:D006332)
- **Chemicals:** PMA (MESH:D013755), xylazine (MESH:D014991), 64Cu (MESH:C000615411), Triton-X100 (MESH:D017830), acetonitrile (MESH:C032159), NaCl (MESH:D012965), TX-100 (MESH:C551282), T (MESH:D014316), oxygen (MESH:D010100), acetic acid (MESH:D019342), copper- (MESH:D003300), CaCl2 (MESH:D002122), Sodium Azide (MESH:D019810), water (MESH:D014867), TBS (MESH:D013725), isoflurane (MESH:D007530), -peptide (MESH:D010455), PSR (MESH:C009798), Fluorescein (MESH:D019793), Alexa Fluor  488 (MESH:C000711379), Cy5.5-T-Peptide (-), sodium citrate (MESH:D000077559), PBS (MESH:D007854), BCA (MESH:C047117), EP-3533 (MESH:C000706187), PFA (MESH:C003043)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985), HT-1080 — Homo sapiens (Human), Fibrosarcoma, Cancer cell line (CVCL_0317)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12912425/full.md

## References

4 references — full list in the complete paper: https://tomesphere.com/paper/PMC12912425/full.md

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Source: https://tomesphere.com/paper/PMC12912425