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Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery.
Ting, Joey P; Tung, Frances; Antonysamy, Stephen; Wasserman, Stephen; Jones, Spencer B; Zhang, Feiyu F; Espada, Alfonso; Broughton, Howard; Chalmers, Michael J; Woodman, Michael E; Bina, Holly A; Dodge, Jeffrey A; Benach, Jordi; Zhang, Aiping; Groshong, Christopher; Manglicmot, Danalyn; Russell, Marijane; Afshar, Sepideh.
Afiliação
  • Ting JP; Department of protein Engineering, Eli Lilly Biotechnology Center, San Diego, California, United States of America.
  • Tung F; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Antonysamy S; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Wasserman S; Department of structural Biology, Discovery Chemistry Research and Technologies, Eli Lilly and Company, Advanced Photon Source, Argonne, Illinois, United States of America.
  • Jones SB; Lilly Research Laboratories, Indianapolis, Indiana, United States of America.
  • Zhang FF; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Espada A; Centro de Investigación Lilly, Alcobendas, Spain.
  • Broughton H; Centro de Investigación Lilly, Alcobendas, Spain.
  • Chalmers MJ; Lilly Research Laboratories, Indianapolis, Indiana, United States of America.
  • Woodman ME; Lilly Research Laboratories, Indianapolis, Indiana, United States of America.
  • Bina HA; Lilly Research Laboratories, Indianapolis, Indiana, United States of America.
  • Dodge JA; Lilly Research Laboratories, Indianapolis, Indiana, United States of America.
  • Benach J; Department of structural Biology, Discovery Chemistry Research and Technologies, Eli Lilly and Company, Advanced Photon Source, Argonne, Illinois, United States of America.
  • Zhang A; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Groshong C; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Manglicmot D; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Russell M; Department of structural Biology, Discovery Chemistry Research and Technologies, Lilly Biotechnology Center, Eli Lilly and Company, San Diego, California, United States of America.
  • Afshar S; Department of protein Engineering, Eli Lilly Biotechnology Center, San Diego, California, United States of America.
PLoS One ; 13(1): e0190850, 2018.
Article em En | MEDLINE | ID: mdl-29329326
ABSTRACT
To date, IL-17A antibodies remain the only therapeutic approach to correct the abnormal activation of the IL-17A/IL-17R signaling complex. Why is it that despite the remarkable success of IL-17 antibodies, there is no small molecule antagonist of IL-17A in the clinic? Here we offer a unique approach to address this question. In order to understand the interaction of IL-17A with its receptor, we combined peptide discovery using phage display with HDX, crystallography, and functional assays to map and characterize hot regions that contribute to most of the energetics of the IL-17A/IL-17R interaction. These functional maps are proposed to serve as a guide to aid in the development of small molecules that bind to IL-17A and block its interaction with IL-17RA.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Colífagos / Interleucina-17 / Receptores de Interleucina-17 Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peptídeos / Colífagos / Interleucina-17 / Receptores de Interleucina-17 Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article