Cryo-EM structure of TMEM164 reveals distinct phospholipid remodeling mechanisms with anti-ferroptotic potential

Phospholipids in cell membrane provide both regulatory and structural function of a cell. How lipid remodeling regulates cell fate remains less explored. Here we report the cryo-electron microscopy structure of TMEM164 identified by genome-wide CRISPR screen as an anti-ferroptotic factor. The overall architecture reveals a dimer of two 7 transmembrane domain monomers and a metal ion catalytic center with phospholipid substrate in a distinct polyunsaturated fatty acyl (PUFA)-C123 intermediate state. Both loss and gain of its function result in the decline of PUFA-ePE and elevation of C16/18:1-ePE, consequently confer resistance to GPX4 inhibitor RSL3 induced ferroptosis. Mutagenesis studies further validate critical residues for the catalytic center (C123) and the chelates center (E106, Y177 and H181). Through virtual screen and rational design, we identify and test candidate inhibitors for TMEM164, including activity for Montelukast S-enantiomer with 4 order of magnitude higher affinity. Our works not only demonstrates TMEM164 as a membrane lipid remodeler that controls the ferroptotic fate, but also highlights the power of integrating multi-scale platforms to unravel distinct mechanisms and functions.

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Publication Details

Journal
Nature Communications
Published
2025-12-20
DOI
https://doi.org/10.1038/s41467-025-67651-2
Primary Topic
Ferroptosis and cancer prognosis
Type
article
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article

Cryo-EM structure of TMEM164 reveals distinct phospholipid remodeling mechanisms with anti-ferroptotic potential

Yuanyue Shan, Guoqiang Yao, Duanqing Pei, Minjing Ke et al.
Nature Communications
Ferroptosis and cancer prognosis
article

Cryo-EM structure of TMEM164 reveals distinct phospholipid remodeling mechanisms with anti-ferroptotic potential

Yuanyue Shan, Guoqiang Yao, Duanqing Pei, Minjing Ke, Xiaodong Shu, Xinyi Guo, Micky D. Tortorella, Huifeng Chen, Mingfeng Zhang, Ziwei Zhai, Chengchen Zhao, Bo Wang, Ying Li, Mengmeng Zhang, Xiaoxi Li, Meiyu Chen, Zichao Wu, Junqi Kuang
article en

Abstract

Phospholipids in cell membrane provide both regulatory and structural function of a cell. How lipid remodeling regulates cell fate remains less explored. Here we report the cryo-electron microscopy structure of TMEM164 identified by genome-wide CRISPR screen as an anti-ferroptotic factor. The overall architecture reveals a dimer of two 7 transmembrane domain monomers and a metal ion catalytic center with phospholipid substrate in a distinct polyunsaturated fatty acyl (PUFA)-C123 intermediate state. Both loss and gain of its function result in the decline of PUFA-ePE and elevation of C16/18:1-ePE, consequently confer resistance to GPX4 inhibitor RSL3 induced ferroptosis. Mutagenesis studies further validate critical residues for the catalytic center (C123) and the chelates center (E106, Y177 and H181). Through virtual screen and rational design, we identify and test candidate inhibitors for TMEM164, including activity for Montelukast S-enantiomer with 4 order of magnitude higher affinity. Our works not only demonstrates TMEM164 as a membrane lipid remodeler that controls the ferroptotic fate, but also highlights the power of integrating multi-scale platforms to unravel distinct mechanisms and functions.

Nature CommunicationsVol. 17(1)
Zhejiang University of Science and Technology (CN), South China Normal University (CN), Chinese Academy of Sciences (CN), Guangzhou Institutes of Biomedicine and Health (CN), Westlake University (CN), Zhejiang Lab (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 40%
Ferroptosis and cancer prognosis
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