Structural basis for ligand recognition of the human hydroxycarboxylic acid receptor HCAR3

Hydroxycarboxylic acid receptor 3 (HCAR3), a class A G-protein-coupled receptor, is an important cellular energy metabolism sensor with a key role in the regulation of lipolysis in humans. HCAR3 is deeply involved in many physiological processes and serves as a valuable target for the treatment of metabolic diseases, tumors, and immune diseases. Here, we report four cryoelectron microscopy (cryo-EM) structures of human HCAR3-Gi1 complexes with or without agonists: the endogenous ligand 3-hydroxyoctanoic acid, the drug niacin, the highly subtype-specific agonist compound 5c (4-(n-propyl)amino-3-nitrobenzoic acid), and the apo form. Together with mutagenesis and functional analyses, we revealed the recognition mechanisms of HCAR3 for different agonists. In addition, the key residues that determine the ligand selectivity between HCAR2 and HCAR3 were also illuminated. Overall, these findings provide a structural basis for the ligand recognition, activation, and selectivity and G-protein coupling mechanisms of HCAR3, which contribute to the design of HCAR3-targeting drugs with high efficacy and selectivity.

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Publication Details

Journal
Cell Reports
Published
2024-10-19
DOI
https://doi.org/10.1016/j.celrep.2024.114895
Citations
7
Primary Topic
Receptor Mechanisms and Signaling
Type
article
Field-Weighted Citation Impact
1.64

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article

Structural basis for ligand recognition of the human hydroxycarboxylic acid receptor HCAR3

Yang Du, Qinggong Wang, Peiruo Ning, Kaizheng Gong et al.
7 citations
Cell Reports
Receptor Mechanisms and Signaling
1.64
article

Structural basis for ligand recognition of the human hydroxycarboxylic acid receptor HCAR3

Yang Du, Qinggong Wang, Peiruo Ning, Kaizheng Gong, Xufu Xiang, Lizhe Zhu, Xinyu Li, Geng Chen, Aijun Liu, Jiancheng Li, Xin Pan, Binghao Zhang, Chungen Qian, Zhiyi Zhang
article en
7 citations

Abstract

Hydroxycarboxylic acid receptor 3 (HCAR3), a class A G-protein-coupled receptor, is an important cellular energy metabolism sensor with a key role in the regulation of lipolysis in humans. HCAR3 is deeply involved in many physiological processes and serves as a valuable target for the treatment of metabolic diseases, tumors, and immune diseases. Here, we report four cryoelectron microscopy (cryo-EM) structures of human HCAR3-Gi1 complexes with or without agonists: the endogenous ligand 3-hydroxyoctanoic acid, the drug niacin, the highly subtype-specific agonist compound 5c (4-(n-propyl)amino-3-nitrobenzoic acid), and the apo form. Together with mutagenesis and functional analyses, we revealed the recognition mechanisms of HCAR3 for different agonists. In addition, the key residues that determine the ligand selectivity between HCAR2 and HCAR3 were also illuminated. Overall, these findings provide a structural basis for the ligand recognition, activation, and selectivity and G-protein coupling mechanisms of HCAR3, which contribute to the design of HCAR3-targeting drugs with high efficacy and selectivity.

Cell ReportsVol. 43(11)
Guangxi University (CN), Shenzhen University (CN), Chinese University of Hong Kong, Shenzhen (CN), Wuhan National Laboratory for Optoelectronics (CN), Huazhong University of Science and Technology (CN), Yangzhou University (CN)
National Natural Science Foundation of China, Science, Technology and Innovation Commission of Shenzhen Municipality
Openalex Percentile: Top 16%
Receptor Mechanisms and Signaling
1.64
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