Function and structure of bradykinin receptor 2 for drug discovery

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作者
Jin-kang Shen
Hai-tao Zhang
机构
[1] Zhejiang University,Hangzhou Institute of Innovative Medicine, Institute of Pharmacology and Toxicology, Zhejiang Province Key Laboratory of Anti
[2] Zhejiang University School of Medicine,Cancer Drug Research, College of Pharmaceutical Sciences
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关键词
type 2 bradykinin receptor; G protein-coupled receptor; functions; structures; drug discovery;
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摘要
Type 2 bradykinin receptor (B2R) is an essential G protein-coupled receptor (GPCR) that regulates the cardiovascular system as a vasodepressor. Dysfunction of B2R is also closely related to cancers and hereditary angioedema (HAE). Although several B2R agonists and antagonists have been developed, icatibant is the only B2R antagonist clinically used for treating HAE. The recently determined structures of B2R have provided molecular insights into the functions and regulation of B2R, which shed light on structure-based drug design for the treatment of B2R-related diseases. In this review, we summarize the structure and function of B2R in relation to drug discovery and discuss future research directions to elucidate the remaining unknown functions of B2R dimerization.
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页码:489 / 498
页数:9
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