Author
Listed:
- Qingqing Zhao
(Fudan University
Westlake University, Key Laboratory of Structural Biology of Zhejiang Province, State Key Laboratory of Gene Expression, School of Life Sciences
Westlake Laboratory of Life Sciences and Biomedicine
Westlake Institute for Advanced Study, Institute of Biology)
- Shiyi Lin
(Fudan University
Westlake University, Key Laboratory of Structural Biology of Zhejiang Province, State Key Laboratory of Gene Expression, School of Life Sciences
Westlake Laboratory of Life Sciences and Biomedicine
Westlake Institute for Advanced Study, Institute of Biology)
- Hang Kang
(Nantong University, Institute of Reproductive Medicine, Medical school)
- Yanfei Ru
(Westlake Laboratory of Life Sciences and Biomedicine
Westlake University, Key Laboratory of Growth Regulation and Translational Research of Zhejiang Province, School of Life Sciences)
- Qikui Xu
(Westlake University, Key Laboratory of Structural Biology of Zhejiang Province, State Key Laboratory of Gene Expression, School of Life Sciences
Westlake Laboratory of Life Sciences and Biomedicine
Westlake Institute for Advanced Study, Institute of Biology)
- Zijing Yu
(Westlake Laboratory of Life Sciences and Biomedicine
Westlake University, School of Life Sciences)
- Xiaofang Huang
(Yale University, Department of Cellular and Molecular Physiology, Yale School of Medicine)
- Carlo De Rito
(University of Parma, Department of Chemistry, Life Sciences, and Environmental Sustainability)
- Giulia Sassi
(University of Parma, Department of Chemistry, Life Sciences, and Environmental Sustainability)
- Shaojie Wang
(Westlake University, Key Laboratory of Structural Biology of Zhejiang Province, State Key Laboratory of Gene Expression, School of Life Sciences
Westlake Laboratory of Life Sciences and Biomedicine
Westlake Institute for Advanced Study, Institute of Biology)
- Shuya Sun
(Nanjing Medical University, State Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, School of Basic Medical Sciences)
- Rui Sun
(Westlake University, School of Medicine
Westlake Laboratory of Life Sciences and Biomedicine, Westlake Center for Intelligent Proteomics)
- Honghan Cheng
(Westlake University, School of Medicine
Westlake Laboratory of Life Sciences and Biomedicine, Westlake Center for Intelligent Proteomics)
- Yi Zhu
(Westlake University, School of Medicine
Westlake Laboratory of Life Sciences and Biomedicine, Westlake Center for Intelligent Proteomics)
- Mingxi Liu
(Nanjing Medical University, State Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, School of Basic Medical Sciences)
- Yongdeng Zhang
(Westlake Laboratory of Life Sciences and Biomedicine
Westlake University, School of Life Sciences)
- Min Jiang
(Westlake Laboratory of Life Sciences and Biomedicine
Westlake University, Key Laboratory of Growth Regulation and Translational Research of Zhejiang Province, School of Life Sciences)
- Riccardo Percudani
(University of Parma, Department of Chemistry, Life Sciences, and Environmental Sustainability)
- Jean-Ju Chung
(Yale University, Department of Cellular and Molecular Physiology, Yale School of Medicine)
- Xuhui Zeng
(Nantong University, Institute of Reproductive Medicine, Medical school)
- Zhen Yan
(Westlake University, Key Laboratory of Structural Biology of Zhejiang Province, State Key Laboratory of Gene Expression, School of Life Sciences
Westlake Laboratory of Life Sciences and Biomedicine
Westlake Institute for Advanced Study, Institute of Biology)
- Jianping Wu
(Westlake University, Key Laboratory of Structural Biology of Zhejiang Province, State Key Laboratory of Gene Expression, School of Life Sciences
Westlake Laboratory of Life Sciences and Biomedicine
Westlake Institute for Advanced Study, Institute of Biology)
Abstract
Sperm capacitation and fertilization are highly regulated by Ca2+ signaling. CatSper, a sperm-specific calcium channel, plays a crucial role in sperm hyperactivated motility and fertility by mediating Ca2+ influx into sperm. CatSper is the most complicated ion channel known, comprising the pore-forming CATSPER1-4 and multiple auxiliary subunits. However, our previous structural study of mouse CatSper suggests the presence of potential component(s) that remain to be identified. The identity and functional significance of the missing piece(s) of CatSper remain elusive. Here, by combining cryo-EM, mass spectrometry, AlphaFold structure prediction, and coevolutionary analysis, we identify armadillo-like helical domain containing 2 (ARMH2) as a cytosolic component of CatSper. ARMH2 forms a cytosolic ternary subcomplex with EFCAB9 and CATSPERζ, which contributes to the stable assembly of the linear arrangement of CatSper nanodomains along the sperm tail and regulates the pH and Ca2+ sensitivity of the channel. Loss of ARMH2 leads to compromised physiological activation of CatSper, thereby resulting in asthenozoospermia and severe subfertility. These findings show that ARMH2 is crucial for sperm function and provide fresh insights into the composition and functional regulation of CatSper. The integrated methodology employed in identifying ARMH2 also provides valuable approaches for discovering uncharacterized components in other protein complexes.
Suggested Citation
Qingqing Zhao & Shiyi Lin & Hang Kang & Yanfei Ru & Qikui Xu & Zijing Yu & Xiaofang Huang & Carlo De Rito & Giulia Sassi & Shaojie Wang & Shuya Sun & Rui Sun & Honghan Cheng & Yi Zhu & Mingxi Liu & Yo, 2025.
"ARMH2 is a cytosolic component of CatSper crucial for sperm function,"
Nature Communications, Nature, vol. 16(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-65952-0
DOI: 10.1038/s41467-025-65952-0
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