Structure and transport mechanism of the human prostaglandin transporter SLCO2A1

SLCO2A1 is a member of the organic anion transporting polypeptide (OATP) family, which preferentially transports prostaglandins (PGs) into cells and plays a vital role in regulating PGs inactivation and distribution. Dysregulation or genetic mutation of SLCO2A1 is associated with primary hypertrophic osteoarthropathy (PHO) and chronic enteropathy associated with the SLCO2A1 gene (CEAS). Although the biophysical and biochemical properties of SLCO2A1 have been characterized, the precise mechanism by which SLCO2A1 recognizes and transports PGs remains unclear. Here, we present the cryo-electron microscopy structures of human SLCO2A1 in apo and PGE<sub>2</sub>-bound forms, revealing the detailed structural features and structural basis for PGs transport. Fatty acid-like PGE<sub>2</sub> binds in the central cavity, engaging in specific interactions with W565 and two serine residues, which are not conserved in other OATPs. Combined with functional assays and structural comparisons, this study offers mechanistic insights into PGE<sub>2</sub> recognition, substrate selectivity, conformational changes, and pathology of SLCO2A1.

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Publication Details

Journal
Nature Communications
Published
2025-08-30
DOI
https://doi.org/10.1038/s41467-025-63615-8
Citations
3
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
4.87

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article

Structure and transport mechanism of the human prostaglandin transporter SLCO2A1

Guangyuan Lu, Daohua Jiang, Zhanyi Xia, Jun Zhao et al.
3 citations
Nature Communications
Cell Adhesion Molecules Research
4.87
article

Structure and transport mechanism of the human prostaglandin transporter SLCO2A1

Guangyuan Lu, Daohua Jiang, Zhanyi Xia, Jun Zhao, Bowen Zhang, Di Wu, Yingying Du, Haoran Xu
article en
3 citations

Abstract

SLCO2A1 is a member of the organic anion transporting polypeptide (OATP) family, which preferentially transports prostaglandins (PGs) into cells and plays a vital role in regulating PGs inactivation and distribution. Dysregulation or genetic mutation of SLCO2A1 is associated with primary hypertrophic osteoarthropathy (PHO) and chronic enteropathy associated with the SLCO2A1 gene (CEAS). Although the biophysical and biochemical properties of SLCO2A1 have been characterized, the precise mechanism by which SLCO2A1 recognizes and transports PGs remains unclear. Here, we present the cryo-electron microscopy structures of human SLCO2A1 in apo and PGE<sub>2</sub>-bound forms, revealing the detailed structural features and structural basis for PGs transport. Fatty acid-like PGE<sub>2</sub> binds in the central cavity, engaging in specific interactions with W565 and two serine residues, which are not conserved in other OATPs. Combined with functional assays and structural comparisons, this study offers mechanistic insights into PGE<sub>2</sub> recognition, substrate selectivity, conformational changes, and pathology of SLCO2A1.

Nature CommunicationsVol. 16(1)
Anhui Medical University (CN), Chinese Academy of Sciences (CN), FZU ‒ Institute of Physics of the Academy of Sciences of the Czech Republic (CZ), Ningxia Medical University (CN), First Affiliated Hospital of Anhui Medical University (CN), Institute of Physics (CN), National Laboratory for Superconductivity (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Peking University, Beijing Municipal Science and Technology Commission
Openalex Percentile: Top 5%
Cell Adhesion Molecules Research
4.87
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