Progress toward new function and design of extracellular G protein-coupled receptor nanobodies.

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Roman R Schlimgen, Brian F Volkman
{"title":"Progress toward new function and design of extracellular G protein-coupled receptor nanobodies.","authors":"Roman R Schlimgen, Brian F Volkman","doi":"10.1016/j.molpha.2025.100054","DOIUrl":null,"url":null,"abstract":"<p><p>Antibodies have played a pivotal role in G protein-coupled receptor (GPCR) research and drug development. Nanobodies, or variable domain heavy chain-only antibodies, have emerged as a next-generation antibody with unique advantages in targeting GPCRs. The first generation of intracellular nanobodies have been instrumental in stabilizing GPCR structures for crystallography and in enabling in vitro GPCR imaging. More recently, extracellular-targeted nanobodies have demonstrated diverse pharmacological profiles, with the ability to modulate GPCR activity, localization, and downstream signaling. With these newly uncovered functional properties, nanobodies can be viewed not only as structural tools but also as modulators of receptor pharmacology. We highlight recent innovations in extracellular GPCR-targeting nanobodies and assess several approaches to accelerate their development as versatile research tools and therapeutics. SIGNIFICANCE STATEMENT: Nanobodies have emerged as a next-generation antibody platform with distinct advantages for targeting G protein-coupled receptors. This review highlights recent advances in extracellular G protein-coupled receptor-targeting nanobodies and explores innovative strategies to accelerate their development as powerful research tools and therapeutic agents.</p>","PeriodicalId":18767,"journal":{"name":"Molecular Pharmacology","volume":"107 8","pages":"100054"},"PeriodicalIF":3.0000,"publicationDate":"2025-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.molpha.2025.100054","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Antibodies have played a pivotal role in G protein-coupled receptor (GPCR) research and drug development. Nanobodies, or variable domain heavy chain-only antibodies, have emerged as a next-generation antibody with unique advantages in targeting GPCRs. The first generation of intracellular nanobodies have been instrumental in stabilizing GPCR structures for crystallography and in enabling in vitro GPCR imaging. More recently, extracellular-targeted nanobodies have demonstrated diverse pharmacological profiles, with the ability to modulate GPCR activity, localization, and downstream signaling. With these newly uncovered functional properties, nanobodies can be viewed not only as structural tools but also as modulators of receptor pharmacology. We highlight recent innovations in extracellular GPCR-targeting nanobodies and assess several approaches to accelerate their development as versatile research tools and therapeutics. SIGNIFICANCE STATEMENT: Nanobodies have emerged as a next-generation antibody platform with distinct advantages for targeting G protein-coupled receptors. This review highlights recent advances in extracellular G protein-coupled receptor-targeting nanobodies and explores innovative strategies to accelerate their development as powerful research tools and therapeutic agents.

胞外G蛋白偶联受体纳米体新功能与设计研究进展。
抗体在G蛋白偶联受体(GPCR)研究和药物开发中起着关键作用。纳米抗体,或可变结构域重链抗体,已成为针对gpcr具有独特优势的新一代抗体。第一代细胞内纳米体在稳定晶体学的GPCR结构和实现体外GPCR成像方面发挥了重要作用。最近,细胞外靶向纳米体显示出不同的药理学特征,具有调节GPCR活性、定位和下游信号传导的能力。有了这些新发现的功能特性,纳米体不仅可以被视为结构工具,而且可以被视为受体药理学的调节剂。我们重点介绍了细胞外靶向gpcr纳米体的最新创新,并评估了几种加速其作为多功能研究工具和治疗方法发展的方法。意义声明:纳米体已成为下一代抗体平台,具有靶向G蛋白偶联受体的独特优势。本文综述了细胞外G蛋白偶联受体靶向纳米体的最新进展,并探讨了加速其作为强大的研究工具和治疗剂发展的创新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molecular Pharmacology
Molecular Pharmacology 医学-药学
CiteScore
7.20
自引率
2.80%
发文量
50
审稿时长
3-6 weeks
期刊介绍: Molecular Pharmacology publishes findings derived from the application of innovative structural biology, biochemistry, biophysics, physiology, genetics, and molecular biology to basic pharmacological problems that provide mechanistic insights that are broadly important for the fields of pharmacology and toxicology. Relevant topics include: Molecular Signaling / Mechanism of Drug Action Chemical Biology / Drug Discovery Structure of Drug-Receptor Complex Systems Analysis of Drug Action Drug Transport / Metabolism
×
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:604180095
Book学术官方微信