Structure-based design of macrocyclic peptides to generate functional antibodies against G protein-coupled receptors

G protein-coupled receptors (GPCRs) are critical to a variety of pathophysiological processes, making them attractive targets for the development of drugs or relevant diagnostic tools. Although GPCRs have been successfully targeted with small molecules, the production of reliable anti-GPCR antibodies remains a major challenge. To address this issue, we develop a strategy using macrocyclic peptides designed to mimic the three-dimensional structure of GPCR extracellular loops as immunogens and use the chicken, which is genetically distant from mammals, as an immunization host to produce antigen-specific antibodies. The high-affinity neurotensin receptor type 1 (NTS1), overexpressed in many types of human cancer and associated with poor prognosis, is used as a target. Rational design of macrocyclic epitope mimics and linker selection are achieved using modeling and predictive analysis software tools based on available NTS1 crystal structures. This study particularly highlights the critical role of the linker in peptide macrocyclization, which determines whether antibodies can exert antagonistic activity. Overall, this strategy represents a valuable asset to produce effective spatial anti-GPCR antibodies and holds promise for diagnostic and therapeutic applications.

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Publication Details

Journal
Nature Communications
Published
2025-12-12
DOI
https://doi.org/10.1038/s41467-025-66030-1
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Structure-based design of macrocyclic peptides to generate functional antibodies against G protein-coupled receptors

Philippe Sarret, Laurent Bruneau‐Cossette, Sandra Morissette, Marie-Édith Nepveu-Traversy et al.
Nature Communications
Chemical Synthesis and Analysis
article

Structure-based design of macrocyclic peptides to generate functional antibodies against G protein-coupled receptors

Philippe Sarret, Laurent Bruneau‐Cossette, Sandra Morissette, Marie-Édith Nepveu-Traversy, Rebecca L. Brouillette, Hassan Traboulsi, Pierre‐Luc Boudreault, Billy Breton, Fernand‐Pierre Gendron, Élie Besserer‐Offroy, Alexandre Murza, Simon Gaudreau, Jean‐Michel Longpré, Karyn Kirby, Malihe Hassanzadeh
article en

Abstract

G protein-coupled receptors (GPCRs) are critical to a variety of pathophysiological processes, making them attractive targets for the development of drugs or relevant diagnostic tools. Although GPCRs have been successfully targeted with small molecules, the production of reliable anti-GPCR antibodies remains a major challenge. To address this issue, we develop a strategy using macrocyclic peptides designed to mimic the three-dimensional structure of GPCR extracellular loops as immunogens and use the chicken, which is genetically distant from mammals, as an immunization host to produce antigen-specific antibodies. The high-affinity neurotensin receptor type 1 (NTS1), overexpressed in many types of human cancer and associated with poor prognosis, is used as a target. Rational design of macrocyclic epitope mimics and linker selection are achieved using modeling and predictive analysis software tools based on available NTS1 crystal structures. This study particularly highlights the critical role of the linker in peptide macrocyclization, which determines whether antibodies can exert antagonistic activity. Overall, this strategy represents a valuable asset to produce effective spatial anti-GPCR antibodies and holds promise for diagnostic and therapeutic applications.

Nature CommunicationsVol. 16(1)
Université de Sherbrooke (CA), Inserm (FR), Immune Biosolutions (Canada) (CA), British American Tobacco (Canada) (CA), NEOMED Institute (CA), Université de Caen Normandie (FR)
Université de Sherbrooke, Mitacs, Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, Fonds de Recherche du Québec - Santé, Faculty of Medicine and Health, University of Sydney
Openalex Percentile: Top 64%
Chemical Synthesis and Analysis
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