Fluorescent Peptide Tracers for Simultaneous Oxytocin Receptor Activation and Visualization

M Monika Perisic Böhm (Institute of Biological Chemistry Faculty of Chemistry University of Vienna Vienna Austria) P Predrag Kalaba R Rachel S. Gormal (Clem Jones Centre for Ageing Dementia Research Queensland Brain Institute The University of Queensland Brisbane Australia) M Maja Zupančič (Department of Molecular Neurosciences Center for Brain Research Medical University of Vienna Vienna Austria) A Alexandra Wolf (Department of Molecular Neurosciences Center for Brain Research Medical University of Vienna Vienna Austria) M Mia Juračić (Institute of Biological Chemistry Faculty of Chemistry University of Vienna Vienna Austria) T Thomas Kremsmayr (Institute of Biological Chemistry Faculty of Chemistry University of Vienna Vienna Austria) F Frédéric A. Meunier (Clem Jones Centre for Ageing Dementia Research Queensland Brain Institute The University of Queensland Brisbane Australia) T Thierry Langer C Christian W. Gruber E Erik Keimpema M Markus Muttenthaler (Faculty of Chemistry, Institute of Biological Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria)

Abstract

Abstract The oxytocin receptor (OTR) regulates critical physiological functions and has been implicated in a range of diseases, including psychiatric and neurodevelopmental disorders such as autism spectrum disorder. However, a lack of reliable molecular tools hampers the progress in understanding OTR's mechanistic roles in (patho)physiological processes. In this work, we addressed this gap and developed potent, selective, and bright fluorescent peptide tracers that enable precise spatial and functional investigations of OTR actions. Our tracers showed efficient OTR labeling, activation, and internalization in cellular bioassays in both live and fixed overexpression and primary cell systems, including those subjected to immunocytochemical protocols, highlighting their versatility as reliable new imaging tools. Additionally, they facilitated single‐molecule tracking of OTR with live‐cell super‐resolution microscopy and were able to separate OTR‐positive cells from mixed oxytocin and vasopressin receptor‐containing cell populations via fluorescence‐activated cell sorting, underscoring their wider scope for live‐cell applications. In summary, we developed versatile fluorescent tracers based on the endogenous ligand oxytocin for both live‐cell and post‐hoc imaging that have additional functional capabilities beyond traditional antibody labeling, offering new avenues to explore OTR's role in health and disease.

Article Details

Volume / Issue Vol. 64, Issue 46
Published November 10, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

M

Monika Perisic Böhm

Institute of Biological Chemistry Faculty of Chemistry University of Vienna Vienna Austria

P

Predrag Kalaba

R

Rachel S. Gormal

Clem Jones Centre for Ageing Dementia Research Queensland Brain Institute The University of Queensland Brisbane Australia

M

Maja Zupančič

Department of Molecular Neurosciences Center for Brain Research Medical University of Vienna Vienna Austria

A

Alexandra Wolf

Department of Molecular Neurosciences Center for Brain Research Medical University of Vienna Vienna Austria

M

Mia Juračić

Institute of Biological Chemistry Faculty of Chemistry University of Vienna Vienna Austria

T

Thomas Kremsmayr

Institute of Biological Chemistry Faculty of Chemistry University of Vienna Vienna Austria

F

Frédéric A. Meunier

Clem Jones Centre for Ageing Dementia Research Queensland Brain Institute The University of Queensland Brisbane Australia

T

Thierry Langer

C

Christian W. Gruber

E

Erik Keimpema

M

Markus Muttenthaler

Faculty of Chemistry, Institute of Biological Chemistry, University of Vienna, Währinger Straße 38, 1090 Vienna, Austria