CCR1
趋化因子受体
CCL21型
化学
趋化因子受体
C-C趋化因子受体6型
CCL13型
CCR2型
CCL7型
XCL2型
趋化因子
细胞生物学
生物
受体
生物化学
作者
Lauri Urvas,Esther Kellenberger
标识
DOI:10.1021/acs.jmedchem.3c00352
摘要
The chemokine system is a key player in the functioning of the immune system and a sought-after target for drug candidates. The number of experimental structures of chemokines in complex with chemokine receptors has increased rapidly over the past few years, providing essential information for rational development of chemokine receptor ligands. Here, we perform a comparative analysis of all chemokine–chemokine receptor structures, with the aim of characterizing the molecular recognition processes and highlighting the relationships between chemokine structures and functional processes. The structures show conserved interaction patterns between the chemokine core and the receptor N-terminus, while interactions near ECL2 display subfamily-specific features. Detailed analyses of the interactions of the chemokine N-terminal domain in the 7TM cavities reveal activation mechanisms for CCR5, CCR2, and CXCR2 and a mechanism for biased agonism in CCR1.
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