Nanobodies to Study G Protein-Coupled Receptor Structure and Function

被引:183
|
作者
Manglik, Aashish [1 ]
Kobilka, Brian K. [1 ]
Steyaert, Jan [2 ,3 ]
机构
[1] Stanford Univ, Dept Mol & Cellular Physiol, Stanford, CA 94305 USA
[2] Vrije Univ Brussel, Struct Biol Brussels, B-1050 Brussels, Belgium
[3] Vrije Univ Brussel, VIB Struct Biol Res Ctr, B-1050 Brussels, Belgium
关键词
nanobody; G protein-coupled receptor; conformational plasticity; receptor activation; crystallographic chaperone; intrabody; BETA(2) ADRENERGIC-RECEPTOR; SINGLE-DOMAIN ANTIBODIES; HEAVY-CHAIN ANTIBODIES; CRYSTAL-STRUCTURE; BETA(2)-ADRENERGIC RECEPTOR; DRUG DISCOVERY; 7-TRANSMEMBRANE RECEPTORS; CONFORMATIONAL STATES; TRANSPORTER REVEALS; LIPIDIC MESOPHASES;
D O I
10.1146/annurev-pharmtox-010716-104710
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ligand-induced activation of G protein-coupled receptors (GPCRs) is a key mechanism permitting communication between cells and organs. Enormous progress has recently elucidated the structural and dynamic features of GPCR transmembrane signaling. Nanobodies, the recombinant antigen-binding fragments of camelid heavy-chain-only antibodies, have emerged as important research tools to lock GPCRs in particular conformational states. Active-state stabilizing nanobodies have elucidated several agonist-bound structures of hormone-activated GPCRs and have provided insight into the dynamic character of receptors. Nanobodies have also been used to stabilize transient GPCR transmembrane signaling complexes, yielding the first structural insights into GPCR signal transduction across the cellular membrane. Beyond their in vitro uses, nanobodies have served as conformational biosensors in living systems and have provided novel ways to modulate GPCR function. Here, we highlight several examples of how nanobodies have enabled the study of GPCR function and give insights into potential future uses of these important tools.
引用
收藏
页码:19 / 37
页数:19
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