Selection and characterization of a peptide-based complement modulator targeting C1 of the innate immune system.
Journal
RSC chemical biology
ISSN: 2633-0679
Titre abrégé: RSC Chem Biol
Pays: England
ID NLM: 101768727
Informations de publication
Date de publication:
31 Jul 2024
31 Jul 2024
Historique:
received:
09
04
2024
accepted:
24
06
2024
medline:
2
8
2024
pubmed:
2
8
2024
entrez:
2
8
2024
Statut:
epublish
Résumé
The human complement pathway plays a pivotal role in immune defence, homeostasis, and autoimmunity regulation, and complement-based therapeutics have emerged as promising interventions, with both antagonistic and agonistic approaches being explored. The classical pathway of complement is initiated when the C1 complex binds to hexameric antibody platforms. Recent structural data revealed that C1 binds to small, homogeneous interfaces at the periphery of the antibody platforms. Here, we have developed a novel strategy for complement activation using macrocyclic peptides designed to mimic the interface between antibodies and the C1 complex.
Identifiants
pubmed: 39092440
doi: 10.1039/d4cb00081a
pii: d4cb00081a
pmc: PMC11289891
doi:
Types de publication
Journal Article
Langues
eng
Pagination
787-799Informations de copyright
This journal is © The Royal Society of Chemistry.
Déclaration de conflit d'intérêts
SMWRH, LA, ALB and THS are co-authors on a patent describing the development and use of peptactins. SAKJ declares no competing interests.