Gu Hui, Gu Chaoyi, Du Toit Andre, Yu Wen, Chen Michael W, Struckman Heather L, Silva Jonathan R, Dai Yifan, Ewing Andrew G
Department of Chemistry and Chemical Engineering, Hunan University of Science and Technology, Xiangtan 411201, China.
Department of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg 41390, Sweden.
J Am Chem Soc. 2025 Jul 30;147(30):27020-27029. doi: 10.1021/jacs.5c09338. Epub 2025 Jul 21.
The electrochemical activities of biomolecular condensates represent a new fundamental functioning mechanism in biochemistry and cell biology. However, our understanding of the underlying molecular mechanism and the interfacial field-dependent chemical activities remains limited. This is due to the lack of technology to probe such activities in real time and at a single-condensate level. Stress granules (SGs) are membraneless organelles that form in the cytoplasm to adapt to cell stress, which are found to encapsulate reactive oxygen species (ROS) in our lab. Here, we design and implement a collision-based electrochemical nanosensor that enables probing of the redox activities of SGs at a single-condensate level in live cells. We show that ex-vivo separated SGs drive the redox reactions depending on their own interfacial potentials and the constituents of the solution system. Surprisingly, we found that water molecules, rather than solvated oxygen (the main source of ROS produced by a conventional enzyme reaction in cells), are the main chemical origin of the redox activity of SGs. Finally, we demonstrate the application of this electrochemical nanosensor in real-time probing of the generation of hydrogen peroxide from SGs in mammalian cells and show that the electrochemical environment of the cells can regulate the redox activity of SGs. This work uncovers the likely mechanisms encoding nonenzymatic redox activities of SGs and demonstrates a key fundamental technological capability that can be highly useful in exploring the intracellular electroactive pathways of macroscale assemblies.
生物分子凝聚物的电化学活性代表了生物化学和细胞生物学中一种新的基本功能机制。然而,我们对其潜在分子机制以及界面场依赖的化学活性的理解仍然有限。这是由于缺乏在实时和单凝聚物水平上探测此类活性的技术。应激颗粒(SGs)是在细胞质中形成以适应细胞应激的无膜细胞器,我们实验室发现它们能包裹活性氧(ROS)。在此,我们设计并实现了一种基于碰撞的电化学纳米传感器,能够在活细胞的单凝聚物水平上探测SGs的氧化还原活性。我们表明,体外分离的SGs根据其自身的界面电位和溶液系统的成分驱动氧化还原反应。令人惊讶的是,我们发现水分子而非溶剂化氧(细胞中传统酶反应产生ROS的主要来源)是SGs氧化还原活性的主要化学起源。最后,我们展示了这种电化学纳米传感器在实时探测哺乳动物细胞中SGs产生过氧化氢方面的应用,并表明细胞的电化学环境可以调节SGs的氧化还原活性。这项工作揭示了编码SGs非酶促氧化还原活性的可能机制,并展示了一种关键的基础技术能力,这在探索宏观组装体的细胞内电活性途径方面可能非常有用。