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Mimotopes of calcitonin gene-related peptide (CGRP) screened from Fv-antibody library: antagonists to CGRP receptor

Authors
 Sung, Jeong Soo  ;  Bae, Hyung Eun  ;  Kang, Min-Jung  ;  Jose, Joachim  ;  Lee, Misu  ;  Chu, Min Kyung  ;  Pyun, Jae-Chul 
Citation
 INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, Vol.334(Pt 2), 2025-12 
Article Number
 149080 
Journal Title
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
ISSN
 0141-8130 
Issue Date
2025-12
MeSH
Amino Acid Sequence ; Calcitonin Gene-Related Peptide Receptor Antagonists* / chemistry ; Calcitonin Gene-Related Peptide Receptor Antagonists* / pharmacology ; Calcitonin Gene-Related Peptide* / chemistry ; Calcitonin Gene-Related Peptide* / immunology ; Calcitonin Gene-Related Peptide* / metabolism ; Calcium / metabolism ; Cell Line, Tumor ; Cyclic AMP / metabolism ; Humans ; Molecular Docking Simulation ; Peptide Library ; Protein Binding ; Receptors, Calcitonin Gene-Related Peptide* / chemistry ; Receptors, Calcitonin Gene-Related Peptide* / metabolism ; Single-Chain Antibodies* / chemistry ; Single-Chain Antibodies* / immunology
Keywords
CGRP ; Mimotope ; Antagonist
Abstract
Calcitonin gene-related peptide (CGRP) is a neuropeptide synthesized in the trigeminal ganglion and it has been identified as a key mediator in the pathophysiology of migraine. The monoclonal antibodies and small-molecule antagonists for calcitonin receptor-like receptor (CLR) have been developed for therapeutics for migraine. In this study, the previously screened CGRP mimotopes sequences from Fv-antibody library were prepared as CDR3 peptides, Fv-antibodies, and heavy chains of immunoglobulin G (VH). Among these, the heavy chain-based mimotopes exhibited the highest binding affinity and antagonist activity against the CGRP receptor. To demonstrate the antagonistic activity, the binding of the CGRP mimotopes to the CGRP receptor was evaluated which prevented CGRP from interacting with the receptor, and then the influence from the inhibition of CGRP binding was demonstrated by measuring (1) intracellular cyclic adenosine monophosphate (cAMP) and (2) Ca2+ levels in the human neuroblastoma cell line SK-N-MC. Additionally, the interaction of screened CGRP mimotopes and the CLR was analyzed using a computer-aided docking simulation, and the interaction of CGRP mimotopes were analyzed to be antagonists preventing the binding of intact CGRP to CLR.
Full Text
https://www.sciencedirect.com/science/article/pii/S0141813025096370
DOI
10.1016/j.ijbiomac.2025.149080
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
Yonsei Authors
Chu, Min Kyung(주민경) ORCID logo https://orcid.org/0000-0001-6221-1346
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/209980
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