ARMH2 is a cytosolic component of CatSper crucial for sperm function

Q Qingqing Zhao (State Key Laboratory of Gene Expression, School of Life Sciences, Westlake University) S Shiyi Lin (State Key Laboratory of Gene Expression, School of Life Sciences, Westlake University) H Hang Kang Y Yanfei Ru (Westlake Laboratory of Life Sciences and Biomedicine) Q Qikui Xu Z Zijing Yu X Xiaofang Huang C Carlo De Rito (Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma) G Giulia Sassi S Shaojie Wang S Shuya Sun R Rui Sun H Honghan Cheng Y Yi Zhu M Mingxi Liu Y Yongdeng Zhang M Min Jiang R Riccardo Percudani (Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma) J Jean-Ju Chung X Xuhui Zeng Z Zhen Yan (Shandong Key Laboratory of Environmental Processes and Health, School of Environmental Science and Engineering) J Jianping Wu

Abstract

Abstract Sperm capacitation and fertilization are highly regulated by Ca 2+ signaling. CatSper, a sperm-specific calcium channel, plays a crucial role in sperm hyperactivated motility and fertility by mediating Ca 2+ 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 Ca 2+ 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.

Article Details

Volume / Issue Vol. 16, Issue 1
Published November 21, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (22)

Q

Qingqing Zhao

State Key Laboratory of Gene Expression, School of Life Sciences, Westlake University

S

Shiyi Lin

State Key Laboratory of Gene Expression, School of Life Sciences, Westlake University

H

Hang Kang

Y

Yanfei Ru

Westlake Laboratory of Life Sciences and Biomedicine

Q

Qikui Xu

Z

Zijing Yu

X

Xiaofang Huang

C

Carlo De Rito

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma

G

Giulia Sassi

S

Shaojie Wang

S

Shuya Sun

R

Rui Sun

H

Honghan Cheng

Y

Yi Zhu

M

Mingxi Liu

Y

Yongdeng Zhang

M

Min Jiang

R

Riccardo Percudani

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma

J

Jean-Ju Chung

X

Xuhui Zeng

Z

Zhen Yan

Shandong Key Laboratory of Environmental Processes and Health, School of Environmental Science and Engineering

J

Jianping Wu