蜕皮激素类似物特丁苯并噻与甲壳素酶多靶点 IGR 的新结合模式

{"title":"蜕皮激素类似物特丁苯并噻与甲壳素酶多靶点 IGR 的新结合模式","authors":"","doi":"10.1016/j.aac.2023.11.006","DOIUrl":null,"url":null,"abstract":"<div><p>Tebufenozide, an efficient insect growth regulator (IGR) against lepidopteran pests, presents a novel mode of action with minimal non-target impact. By competing with ecdysteroids for ecdysone receptor (EcR) binding, it regulates insect growth precisely. This study explores tebufenozide's potential as a multitarget IGR, targeting both EcR and <em>Ostrinia furnacalis</em> chitinase I (<em>Of</em>ChtI). The inhibitory activity against <em>Of</em>ChtI is comparable to that of substrates (GlcNAc)<sub>5</sub>, with an IC<sub>50</sub> of 45.77 ​μM. Our computational findings indicate that tebufenozide binds at the subsite −1 to +1 of <em>Of</em>ChtI through various interactions. Notably, tebufenozide establishes a pi-pi interaction with the flipped sidechain of Trp107, enabling tebufenozide to deeply penetrate into the S1 pocket, thereby obstructing substrate binding to <em>Of</em>ChtI. These insights highlight the potency of multitarget strategies, laying the groundwork for innovative IGR designs that offer comprehensive pest management solutions.</p></div>","PeriodicalId":100027,"journal":{"name":"Advanced Agrochem","volume":"3 3","pages":"Pages 229-236"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2773237123000990/pdfft?md5=f82031eab2e4c395013f816903ce225e&pid=1-s2.0-S2773237123000990-main.pdf","citationCount":"0","resultStr":"{\"title\":\"A new binding mode for ecdysteroid analog tebufenozide as a multitargeted IGR with chitinase\",\"authors\":\"\",\"doi\":\"10.1016/j.aac.2023.11.006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Tebufenozide, an efficient insect growth regulator (IGR) against lepidopteran pests, presents a novel mode of action with minimal non-target impact. By competing with ecdysteroids for ecdysone receptor (EcR) binding, it regulates insect growth precisely. This study explores tebufenozide's potential as a multitarget IGR, targeting both EcR and <em>Ostrinia furnacalis</em> chitinase I (<em>Of</em>ChtI). The inhibitory activity against <em>Of</em>ChtI is comparable to that of substrates (GlcNAc)<sub>5</sub>, with an IC<sub>50</sub> of 45.77 ​μM. Our computational findings indicate that tebufenozide binds at the subsite −1 to +1 of <em>Of</em>ChtI through various interactions. Notably, tebufenozide establishes a pi-pi interaction with the flipped sidechain of Trp107, enabling tebufenozide to deeply penetrate into the S1 pocket, thereby obstructing substrate binding to <em>Of</em>ChtI. These insights highlight the potency of multitarget strategies, laying the groundwork for innovative IGR designs that offer comprehensive pest management solutions.</p></div>\",\"PeriodicalId\":100027,\"journal\":{\"name\":\"Advanced Agrochem\",\"volume\":\"3 3\",\"pages\":\"Pages 229-236\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-11-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2773237123000990/pdfft?md5=f82031eab2e4c395013f816903ce225e&pid=1-s2.0-S2773237123000990-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Agrochem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2773237123000990\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Agrochem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773237123000990","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

特丁苯酰菌胺是一种高效的昆虫生长调节剂(IGR),可防治鳞翅目害虫,其作用模式新颖,对非目标影响最小。通过与蜕皮激素竞争蜕皮激素受体(EcR)的结合,它可以精确地调节昆虫的生长。本研究探讨了特丁苯并噻唑作为多靶点 IGR 的潜力,它同时针对 EcR 和 Ostrinia furnacalis 几丁质酶 I(OfChtI)。它对 OfChtI 的抑制活性与底物(GlcNAc)5 相当,IC50 为 45.77 μM。我们的计算结果表明,特丁福诺嗪通过各种相互作用与 OfChtI 的位点 -1 至 +1 结合。值得注意的是,特丁福诺嗪与Trp107的翻转侧链建立了pi-pi相互作用,使特丁福诺嗪能够深入S1口袋,从而阻碍底物与OfChtI结合。这些见解凸显了多靶标策略的功效,为提供全面虫害管理解决方案的创新 IGR 设计奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A new binding mode for ecdysteroid analog tebufenozide as a multitargeted IGR with chitinase

A new binding mode for ecdysteroid analog tebufenozide as a multitargeted IGR with chitinase

Tebufenozide, an efficient insect growth regulator (IGR) against lepidopteran pests, presents a novel mode of action with minimal non-target impact. By competing with ecdysteroids for ecdysone receptor (EcR) binding, it regulates insect growth precisely. This study explores tebufenozide's potential as a multitarget IGR, targeting both EcR and Ostrinia furnacalis chitinase I (OfChtI). The inhibitory activity against OfChtI is comparable to that of substrates (GlcNAc)5, with an IC50 of 45.77 ​μM. Our computational findings indicate that tebufenozide binds at the subsite −1 to +1 of OfChtI through various interactions. Notably, tebufenozide establishes a pi-pi interaction with the flipped sidechain of Trp107, enabling tebufenozide to deeply penetrate into the S1 pocket, thereby obstructing substrate binding to OfChtI. These insights highlight the potency of multitarget strategies, laying the groundwork for innovative IGR designs that offer comprehensive pest management solutions.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.50
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信