Two‐Nanosensor Electrochemical Profiling of Catecholamine Vesicle Interactions With Acute and Chronic Stress Granules in Living Cells

H Hui Gu (Department of Chemistry and Chemical Engineering) C Chaoyi Gu (Department of Chemistry and Molecular Biology) A Andre Du Toit (Department of Chemistry and Molecular Biology) A Andrew G. Ewing (Department of Chemistry and Molecular Biology)

Abstract

ABSTRACT Stress granules (SGs) are dynamic, membrane‐less condensates that assemble in response to stress and have been increasingly linked to neurodegenerative disease (NDD) pathology. However, the molecular and functional mechanisms by which stress granules interact with other cellular organelles remain poorly understood. Here, we present a two‐nanosensor electrochemical strategy that enables quantitative discrimination of reactive oxygen species (ROS) in SGs and catecholamines in vesicles at single‐cell resolution. Using this approach, we distinguished the intracellular effects of acute and chronic SGs in catecholaminergic cells. Chronic SGs induced by prolonged cisplatin stress, contained elevated ROS levels and markedly increased catecholamine storage per vesicle, likely through ROS‐mediated homotypic vesicle fusion. In contrast, acute SGs induced by arsenite exhibited negligible effects. We further demonstrate that chronic SGs exhibit features of aged SGs, such as slow ROS release and enhanced redox activity. These results uncover a redox‐coupled SG‐vesicle interplay modulated by SG aging and identify chronic SGs as endogenous redox‐active condensates that may contribute to neurotransmitter dysregulation and neurodegeneration.

Article Details

Volume / Issue Vol. 65, Issue 15
Published April 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (4)

H

Hui Gu

Department of Chemistry and Chemical Engineering

C

Chaoyi Gu

Department of Chemistry and Molecular Biology

A

Andre Du Toit

Department of Chemistry and Molecular Biology

A

Andrew G. Ewing

Department of Chemistry and Molecular Biology