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Collagen hybridizing peptide to target in vivo misfolded collagen in OI zebrafish
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  • Published: 06 May 2026

Collagen hybridizing peptide to target in vivo misfolded collagen in OI zebrafish

  • Francesca Tonelli1,
  • Carla Aresi1,
  • Cecilia Masiero1,
  • Roberta Gioia3,
  • Tian Morrison4,
  • Antonio Rossi1,
  • S. Michael Yu4 &
  • …
  • Antonella Forlino1,2 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biological techniques
  • Biotechnology
  • Diseases
  • Medical research

Abstract

Osteogenesis imperfecta (OI) is a heritable connective tissue disorder characterized by defects in collagen I, leading to increased bone fragility and turnover. The zebrafish Chihuahua (Chi/+), carrying a p.(Gly736Asp) substitution in the α1(I) chain, recapitulates key features of human OI, including the presence of misfolded collagen I in extracellular matrix. In this study, we evaluated the specificity of a fluorescently labeled collagen hybridizing peptide (Cy5-CHP) for detecting in vivo misfolded collagen I in adult zebrafish. The CHP or the scrambled control peptides were injected intraperitoneally into WT and Chi/+ zebrafish, and average radiant efficiency was quantified at 24 and 72 h post-injection (hpi) in the vertebral column, cranium and heart, representing collagen I–rich organs, as well as the brain, a collagen I–poor tissue. Our results revealed Cy5-CHP specific binding to collagen I-rich tissues in Chi/+ zebrafish at 24 hpi, with minimal signal in the brain, whereas low signal was detectable across all tissues in WT. Cy5-CHP fluorescence was reduced by 72 hpi in all samples, consistent with the low binding affinity of the peptide. Histological analyses confirmed the co-localization of Cy5-CHP with collagen fibers in the endplates of Chi/+ vertebrae at 24 hpi. These findings provide the first in vivo evidence in zebrafish that Cy5-CHP selectively binds misfolded collagen, showing preferential accumulation in collagen I–rich tissues in OI. Overall, the results support the use of Cy5-CHP as a sensitive tool for detecting pathologic collagen and as a potential platform for tissue-targeted drug delivery in OI and other collagen-related disorders.

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Abbreviations

ARE:

Average Radiant Efficiency

Chi/+:

Chihuahua

CHP:

Collagen Hybridizing Peptide

DMSO:

Dimethyl Sulfoxide

ECM:

Extracellular Matrix

EDTA:

Ethylenediaminetetraacetic Acid

ER:

Endoplasmic Reticulum

hpi:

hours post injection

i.p.:

intraperitoneal injection

IVDs:

Intervertebral Endplate Disks

OI:

Osteogenesis Imperfecta

PFA:

Paraformaldeyde

RP-HPLC:

Reverse-Phase High Performance Liquid Chromatography

ROIs:

Regions Of Interest

4PBA:

4-Phenylbutyrate

Acknowledgements

We thank the Health Science Center Core at the University of Utah Health Sciences Centers for ESI-MS experiments performed by using equipment provided for by University of Utah RIF funds. We thank the animal facility “Centro di servizio per la gestione unificata delle attività di stabulazione e di radi¬obiologia” of the University of Pavia, Pavia, Italy, for animal care. We acknowledge Centro Grandi Strumenti and the Optical Microscopy Facility of the University of Pavia, Italy, in particular Dr.Amanda Oldani and Dr.Patrizia Vaghi for their support and assistance in this work.

Funding

This work was supported by Italian Ministry of Education, University and Research (MIUR) [Dipartimenti di Eccellenza (2023–2027)] to AF; by Regione Lombardia, “regionallawn°9/2020, resolutionn°3776/202000 to AF; by the European Union’s - Next Generation EU’’ program through the Italian PRIN 2022 - M4C2, Investimento 1.1 - grant n. 20223C8C5B - CUP F53D23006870006 to AF and in part by the NIH (R01AR084689) and the Fulbright US Scholar Award awarded to S.M.Y.

Author information

Authors and Affiliations

  1. Department of Molecular Medicine, Biochemistry Unit, University of Pavia, Via Taramelli 3/b, Pavia, 27100, Italy

    Francesca Tonelli, Carla Aresi, Cecilia Masiero, Antonio Rossi & Antonella Forlino

  2. Research Platform, IRCCS San Matteo, Pavia, Italy

    Antonella Forlino

  3. Biomedical Imaging Laboratory, Centro Grandi Strumenti, University of Pavia, Pavia, Italy

    Roberta Gioia

  4. Department of Biomedical Engineering, University of Utah, Salt Lake City, UT, USA

    Tian Morrison & S. Michael Yu

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  1. Francesca Tonelli
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  2. Carla Aresi
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  3. Cecilia Masiero
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  7. S. Michael Yu
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  8. Antonella Forlino
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Corresponding author

Correspondence to Antonella Forlino.

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Cite this article

Tonelli, F., Aresi, C., Masiero, C. et al. Collagen hybridizing peptide to target in vivo misfolded collagen in OI zebrafish. Sci Rep (2026). https://doi.org/10.1038/s41598-026-51282-8

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  • Received: 16 February 2026

  • Accepted: 27 April 2026

  • Published: 06 May 2026

  • DOI: https://doi.org/10.1038/s41598-026-51282-8

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Keywords

  • Osteogenesis imperfecta
  • Misfolded collagen
  • Bone
  • CHP
  • Zebrafish
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