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Recruitment pharmacophore for interleukin 5 receptor α antagonism
Author(s) -
Bhattacharya Madhushree,
Pillalamari Udaya,
Sarkhel Sanjay,
Ishino Tetsuya,
Urbina Cecilia,
Jameson Bradford,
Chaiken Irwin
Publication year - 2006
Publication title -
peptide science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.20612
Subject(s) - pharmacophore , chemistry , peptide , hydrogen bond , receptor , antagonism , stereochemistry , steric effects , docking (animal) , amino acid , protein structure , biochemistry , molecule , organic chemistry , medicine , nursing
Abstract Interleukin‐5 receptor α is a therapeutic target for hypereosinophilic diseases including allergic inflammations and asthma. The cyclic peptide AF17121 (Ac‐VDE[CWRIIASHTWFC]AEE‐CONH 2 ) has been identified as a submicromolar inhibitor of interleukin 5 (IL5)‐interleukin 5 receptor α (IL5Rα) interaction from a random peptide screen. However, this inhibitor has limitations as a drug lead because of its relatively large size. We used chemical synthesis of peptides with natural and non‐natural amino acids along with kinetic binding and cell proliferation competition assays to expand definition of structural elements in the peptide that are important for receptor antagonism and to elucidate the underlying pharmacophore. We found that the specific steric array of hydrogen bonding groups in the Arg 6 guanido side chain is critical for receptor inhibition. We also investigated noncharged structural elements in AF17121. Screening a set of five hydrophobic residues showed that peptide function is strongly sensitive to variations in several of these residues, most prominently Ile 7 and Trp 13. We postulate that presentation of charged, hydrogen bonding and hydrophobic structural elements within the disulfide‐constrained peptide drives IL5Rα recruitment by AF17121. We hypothesize from these results and previous receptor mutagenesis studies that Arg 6 recruitment of IL5Rα occurs through hydrogen bonding as well as charge–charge interactions with Asp 55 in site one of domain 1 of IL5Rα, and that this interaction is complemented by additional charged and hydrophobic interactions around the Asp 55 locus. Scaffolding a limited set of structural elements in the inhibitor pharmacophore may be useful for small molecule antagonist design inspired by the peptide. © 2006 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 88:83–93, 2007. This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com.