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Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery
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...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766103/ https://www.ncbi.nlm.nih.gov/pubmed/29329326 http://dx.doi.org/10.1371/journal.pone.0190850 |
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author | 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 |
author_facet | 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 |
author_sort | Ting, Joey P. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5766103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57661032018-01-23 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 PLoS One Research Article 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. Public Library of Science 2018-01-12 /pmc/articles/PMC5766103/ /pubmed/29329326 http://dx.doi.org/10.1371/journal.pone.0190850 Text en © 2018 Ting et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article 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 Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery |
title | Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery |
title_full | Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery |
title_fullStr | Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery |
title_full_unstemmed | Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery |
title_short | Utilization of peptide phage display to investigate hotspots on IL-17A and what it means for drug discovery |
title_sort | utilization of peptide phage display to investigate hotspots on il-17a and what it means for drug discovery |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766103/ https://www.ncbi.nlm.nih.gov/pubmed/29329326 http://dx.doi.org/10.1371/journal.pone.0190850 |
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