A genetically encoded ionic-stress sensor reveals protons as a sleep driver

Dynamic ionic changes are hallmarks of physiological and behavioral state transitions, including sleep in animals. Although biosensors for specific cellular ions are widely available, real-time monitoring of overall ionic strength in living organisms remains challenging. Here, we present a genetically encoded nuclear translocation ionic sensor (GENTIS) that enables direct visualization of ionic stress <i>in vivo</i>. Using GENTIS in <i>C. elegans</i>, we uncover rhythmic elevations in ionic strength during larval molting transitions that coincide with the lethargus sleep. Cytosolic proton ionic increase through inhibition of v-ATPase is sufficient to induce GENTIS nuclear translocation and evoke behavioral quiescence, characterized by reduced feeding and activation of sleep-active neurons. Apical membrane v-ATPases undergo disassembly during lethargus and under sleep-inducing stress conditions, leading to proton accumulation. Notably, this proton-mediated sleep is suppressed by proton buffering with ammonium. Together, these findings establish GENTIS as a powerful tool for tracking ionic strength dynamics in living organisms and support protons as a physiological driver of sleep.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-30
DOI
https://doi.org/10.64898/2026.01.27.702131
Primary Topic
ATP Synthase and ATPases Research
Type
article
Field-Weighted Citation Impact
0.00

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article

A genetically encoded ionic-stress sensor reveals protons as a sleep driver

Zhijian Ji, K. Dengke, Xiaokun Shu, Jianxiu Zhang et al.
bioRxiv (Cold Spring Harbor Laboratory)
ATP Synthase and ATPases Research
article

A genetically encoded ionic-stress sensor reveals protons as a sleep driver

Zhijian Ji, K. Dengke, Xiaokun Shu, Jianxiu Zhang, Junqiang Liu, Bingying Wang, Wenjie Zeng, Chan-I Chung, Zhimin Ma, Yanchang Bian, Shuaian Wei
article en

Abstract

Dynamic ionic changes are hallmarks of physiological and behavioral state transitions, including sleep in animals. Although biosensors for specific cellular ions are widely available, real-time monitoring of overall ionic strength in living organisms remains challenging. Here, we present a genetically encoded nuclear translocation ionic sensor (GENTIS) that enables direct visualization of ionic stress <i>in vivo</i>. Using GENTIS in <i>C. elegans</i>, we uncover rhythmic elevations in ionic strength during larval molting transitions that coincide with the lethargus sleep. Cytosolic proton ionic increase through inhibition of v-ATPase is sufficient to induce GENTIS nuclear translocation and evoke behavioral quiescence, characterized by reduced feeding and activation of sleep-active neurons. Apical membrane v-ATPases undergo disassembly during lethargus and under sleep-inducing stress conditions, leading to proton accumulation. Notably, this proton-mediated sleep is suppressed by proton buffering with ammonium. Together, these findings establish GENTIS as a powerful tool for tracking ionic strength dynamics in living organisms and support protons as a physiological driver of sleep.

bioRxiv (Cold Spring Harbor Laboratory)
University of California, San Francisco (US), Innovative Genomics Institute (US), University of California, Berkeley (US), Stanford University (US)
American Heart Association, Tokyo Women's Medical University, National Institutes of Health, University of California, San Francisco
Openalex Percentile: Top 73%
ATP Synthase and ATPases Research
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