Structural insights into AQP3 channel closure upon pH and redox changes reveal an autoregulatory molecular mechanism

Regulation of intracellular levels of reactive oxygen species (ROS) remains poorly understood. Aquaporin 3 (AQP3) facilitates the membrane transport of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), a key ROS signaling molecule. Here we elucidate the molecular mechanism of AQP3 and show that its regulatory properties are both pH dependent and autoregulated by H<sub>2</sub>O<sub>2</sub>. Using single particle cryo-electron microscopy, we present open and closed conformations of human AQP3. At pH 8.0, the channel adopts an open state, while acidic pH or exposure to H<sub>2</sub>O<sub>2</sub> promotes closure via a large conformational rearrangement of extracellular loop E. These findings reveal a mechanism for autoregulation of H<sub>2</sub>O<sub>2</sub> transport and establish AQP3 as a key modulator of redox homeostasis in human pancreatic β-cells.

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Publication Details

Journal
Nature Communications
Published
2025-12-22
DOI
https://doi.org/10.1038/s41467-025-67144-2
Primary Topic
Ion Transport and Channel Regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Structural insights into AQP3 channel closure upon pH and redox changes reveal an autoregulatory molecular mechanism

Isabella Artner, Carter J. Wilson, Pontus Gourdon, Sara Bsharat et al.
Nature Communications
Ion Transport and Channel Regulation
article

Structural insights into AQP3 channel closure upon pH and redox changes reveal an autoregulatory molecular mechanism

Isabella Artner, Carter J. Wilson, Pontus Gourdon, Sara Bsharat, Peng Huang, Rashmi B Prasad, Lindkvist-Petersson Karin, Raminta Venskutonytė, Bert L. de Groot
article en

Abstract

Regulation of intracellular levels of reactive oxygen species (ROS) remains poorly understood. Aquaporin 3 (AQP3) facilitates the membrane transport of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), a key ROS signaling molecule. Here we elucidate the molecular mechanism of AQP3 and show that its regulatory properties are both pH dependent and autoregulated by H<sub>2</sub>O<sub>2</sub>. Using single particle cryo-electron microscopy, we present open and closed conformations of human AQP3. At pH 8.0, the channel adopts an open state, while acidic pH or exposure to H<sub>2</sub>O<sub>2</sub> promotes closure via a large conformational rearrangement of extracellular loop E. These findings reveal a mechanism for autoregulation of H<sub>2</sub>O<sub>2</sub> transport and establish AQP3 as a key modulator of redox homeostasis in human pancreatic β-cells.

Nature CommunicationsVol. 16(1)
Lund University (SE), Engineering Link (Canada) (CA), Max Planck Institute for Dynamics and Self-Organization (DE), Tissue Dynamics (Israel) (IL)
Kempe Foundation, Cancerfonden, Lunds Universitet, Vetenskapsrådet, China Scholarship Council, Umeå Universitet, Kempestiftelserna, Diabetesfonden, Stockholms Universitet, Science for Life Laboratory, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 37%
Ion Transport and Channel Regulation
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