GPCR-targeting nanobodies: attractive research tools, diagnostics, and therapeutics

被引:73
作者
Mujic-Delic, Azra [1 ]
de Wit, Raymond H. [1 ]
Verkaar, Folkert [1 ]
Smit, Martine J. [1 ]
机构
[1] Vrije Univ Amsterdam, Fac Sci, AIMMS, Div Med Chem, NL-1081 HV Amsterdam, Netherlands
关键词
GPCRs; nanobodies; VHH; single-domain antibody; signaling; MONOCYTE CHEMOATTRACTANT PROTEIN-1; MACROPHAGE MANNOSE RECEPTOR; DOMAIN ANTIBODY FRAGMENTS; CHEMOKINE RECEPTORS; MULTIPLE-SCLEROSIS; CRYSTAL-STRUCTURE; OLIGOMERIZATION; EXPRESSION; BINDING; CXCR4;
D O I
10.1016/j.tips.2014.03.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G-protein-coupled receptors (GPCRs) represent a major therapeutic target class. A large proportion of marketed drugs exert their effect through modulation of GPCR function, and GPCRs have been successfully targeted with small molecules. Yet, the number of small new molecular entities targeting GPCRs that has been approved as therapeutics in the past decade has been limited. With new and improved immunization-related technologies and advances in GPCR purification and expression techniques, antibody-based targeting of GPCRs has gained attention. The serendipitous discovery of a unique class of heavy chain antibodies (hcAbs) in the sera of camelids may provide novel GPCR-directed therapies. Antigen-binding fragments of hcAbs, also referred to as nanobodies, combine the advantages of both small molecules (e.g., molecular cavity binding, low production costs) and monoclonal antibodies (e.g., high affinity and specificity). Nanobodies are gaining ground as therapeutics and are also starting to find application as diagnostics and as high-quality tools in GPCR research. Herein, we review recent advances in the use of nanobodies in GPCR research.
引用
收藏
页码:247 / 255
页数:9
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