Cargando…
Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP
The ecdysone receptor (EcR) possesses the remarkable capacity to adapt structurally to different types of ligands. EcR binds ecdysteroids, including 20-hydroxyecdysone (20E), as well as nonsteroidal synthetic agonists such as insecticidal dibenzoylhydrazines (DBHs). Here, we report the crystal struc...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pesticide Science Society of Japan
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953031/ https://www.ncbi.nlm.nih.gov/pubmed/33746550 http://dx.doi.org/10.1584/jpestics.D20-095 |
_version_ | 1783663849095823360 |
---|---|
author | Browning, Christopher McEwen, Alastair G. Mori, Kotaro Yokoi, Taiyo Moras, Dino Nakagawa, Yoshiaki Billas, Isabelle M. L. |
author_facet | Browning, Christopher McEwen, Alastair G. Mori, Kotaro Yokoi, Taiyo Moras, Dino Nakagawa, Yoshiaki Billas, Isabelle M. L. |
author_sort | Browning, Christopher |
collection | PubMed |
description | The ecdysone receptor (EcR) possesses the remarkable capacity to adapt structurally to different types of ligands. EcR binds ecdysteroids, including 20-hydroxyecdysone (20E), as well as nonsteroidal synthetic agonists such as insecticidal dibenzoylhydrazines (DBHs). Here, we report the crystal structures of the ligand-binding domains of Heliothis virescens EcR/USP bound to the DBH agonist BYI09181 and to the imidazole-type compound BYI08346. The region delineated by helices H7 and H10 opens up to tightly fit a phenyl ring of the ligands to an extent that depends on the bulkiness of ring substituent. In the structure of 20E-bound EcR, this part of the ligand-binding pocket (LBP) contains a channel filled by water molecules that form an intricate hydrogen bond network between 20E and LBP. The water channel present in the nuclear receptor bound to its natural hormone acts as a critical molecular adaptation spring used to accommodate synthetic agonists inside its binding cavity. |
format | Online Article Text |
id | pubmed-7953031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Pesticide Science Society of Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-79530312021-03-18 Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP Browning, Christopher McEwen, Alastair G. Mori, Kotaro Yokoi, Taiyo Moras, Dino Nakagawa, Yoshiaki Billas, Isabelle M. L. J Pestic Sci Regular Article The ecdysone receptor (EcR) possesses the remarkable capacity to adapt structurally to different types of ligands. EcR binds ecdysteroids, including 20-hydroxyecdysone (20E), as well as nonsteroidal synthetic agonists such as insecticidal dibenzoylhydrazines (DBHs). Here, we report the crystal structures of the ligand-binding domains of Heliothis virescens EcR/USP bound to the DBH agonist BYI09181 and to the imidazole-type compound BYI08346. The region delineated by helices H7 and H10 opens up to tightly fit a phenyl ring of the ligands to an extent that depends on the bulkiness of ring substituent. In the structure of 20E-bound EcR, this part of the ligand-binding pocket (LBP) contains a channel filled by water molecules that form an intricate hydrogen bond network between 20E and LBP. The water channel present in the nuclear receptor bound to its natural hormone acts as a critical molecular adaptation spring used to accommodate synthetic agonists inside its binding cavity. Pesticide Science Society of Japan 2021-02-20 /pmc/articles/PMC7953031/ /pubmed/33746550 http://dx.doi.org/10.1584/jpestics.D20-095 Text en © 2021 Pesticide Science Society of Japan https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) License. |
spellingShingle | Regular Article Browning, Christopher McEwen, Alastair G. Mori, Kotaro Yokoi, Taiyo Moras, Dino Nakagawa, Yoshiaki Billas, Isabelle M. L. Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP |
title | Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP |
title_full | Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP |
title_fullStr | Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP |
title_full_unstemmed | Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP |
title_short | Nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex EcR/USP |
title_sort | nonsteroidal ecdysone receptor agonists use a water channel for binding to the ecdysone receptor complex ecr/usp |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7953031/ https://www.ncbi.nlm.nih.gov/pubmed/33746550 http://dx.doi.org/10.1584/jpestics.D20-095 |
work_keys_str_mv | AT browningchristopher nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp AT mcewenalastairg nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp AT morikotaro nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp AT yokoitaiyo nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp AT morasdino nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp AT nakagawayoshiaki nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp AT billasisabelleml nonsteroidalecdysonereceptoragonistsuseawaterchannelforbindingtotheecdysonereceptorcomplexecrusp |