可靶向G蛋白蛋白质组:下一代药物靶点在哪里?

R.Victor Rebois , Bruce G. Allen, Terence E. Hébert
{"title":"可靶向G蛋白蛋白质组:下一代药物靶点在哪里?","authors":"R.Victor Rebois ,&nbsp;Bruce G. Allen,&nbsp;Terence E. Hébert","doi":"10.1016/S1741-8372(04)02429-6","DOIUrl":null,"url":null,"abstract":"<div><p>G protein-coupled signaling systems are the most important targets for therapeutic drugs, most of which are ligands for heptahelical receptors (7TM-R). A single receptor can activate various signaling pathways<span> in different cells; consequently, drugs that target the receptor binding site are not necessarily specific for particular pathways. However, other downstream signaling partners that interact with heptahelical receptors can be unique for a given pathway and peptide motifs that are involved in these interactions are potential targets for the development of drugs with greater specificity and fewer side effects. Furthermore, it is becoming apparent that these systems are organized as protein complexes<span>, making proteomic techniques ideal tools for identifying system components.</span></span></p></div>","PeriodicalId":100382,"journal":{"name":"Drug Discovery Today: TARGETS","volume":"3 3","pages":"Pages 104-111"},"PeriodicalIF":0.0000,"publicationDate":"2004-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1741-8372(04)02429-6","citationCount":"6","resultStr":"{\"title\":\"The targetable G protein proteome: where is the next generation of drug targets?\",\"authors\":\"R.Victor Rebois ,&nbsp;Bruce G. Allen,&nbsp;Terence E. Hébert\",\"doi\":\"10.1016/S1741-8372(04)02429-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>G protein-coupled signaling systems are the most important targets for therapeutic drugs, most of which are ligands for heptahelical receptors (7TM-R). A single receptor can activate various signaling pathways<span> in different cells; consequently, drugs that target the receptor binding site are not necessarily specific for particular pathways. However, other downstream signaling partners that interact with heptahelical receptors can be unique for a given pathway and peptide motifs that are involved in these interactions are potential targets for the development of drugs with greater specificity and fewer side effects. Furthermore, it is becoming apparent that these systems are organized as protein complexes<span>, making proteomic techniques ideal tools for identifying system components.</span></span></p></div>\",\"PeriodicalId\":100382,\"journal\":{\"name\":\"Drug Discovery Today: TARGETS\",\"volume\":\"3 3\",\"pages\":\"Pages 104-111\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2004-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1741-8372(04)02429-6\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug Discovery Today: TARGETS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1741837204024296\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Discovery Today: TARGETS","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1741837204024296","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

摘要

G蛋白偶联信号系统是治疗药物最重要的靶点,其中大多数是七螺旋受体(7TM-R)的配体。一个受体可以激活不同细胞中的多种信号通路;因此,靶向受体结合位点的药物不一定针对特定途径。然而,与七螺旋受体相互作用的其他下游信号伙伴对于给定的途径可能是独特的,参与这些相互作用的肽基序是开发具有更大特异性和更少副作用的药物的潜在靶标。此外,越来越明显的是,这些系统是由蛋白质复合物组成的,这使得蛋白质组学技术成为识别系统组件的理想工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The targetable G protein proteome: where is the next generation of drug targets?

G protein-coupled signaling systems are the most important targets for therapeutic drugs, most of which are ligands for heptahelical receptors (7TM-R). A single receptor can activate various signaling pathways in different cells; consequently, drugs that target the receptor binding site are not necessarily specific for particular pathways. However, other downstream signaling partners that interact with heptahelical receptors can be unique for a given pathway and peptide motifs that are involved in these interactions are potential targets for the development of drugs with greater specificity and fewer side effects. Furthermore, it is becoming apparent that these systems are organized as protein complexes, making proteomic techniques ideal tools for identifying system components.

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
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