Ma Qianqian, Han Xiao, Zhu Kexin, Ng Cai Xin, He Danxia, Miao Yansong
School of Biological Sciences, Nanyang Technological University, Singapore 637551, Singapore.
Institute for Digital Molecular Analytics and Science, Nanyang Technological University, Singapore 636921, Singapore.
Proc Natl Acad Sci U S A. 2025 Jul 22;122(29):e2420467122. doi: 10.1073/pnas.2420467122. Epub 2025 Jul 16.
The dynamic organization of the actin cytoskeleton, crucial for numerous cellular processes, is intricately regulated by the nucleotide state of actin filaments (F-actin). Visualization tools for specifically detecting ADP-bound F-actin, however, remain limited. Here, we introduce ADPact, a 20-amino-acid peptide that selectively binds to ADP-F-actin. ADPact allows for the precise visualization of ADP-F-actin structures both in vitro and in eukaryotic cells, particularly under energy stress conditions where ADP-/ATP-actin ratio increases. Importantly, ADPact and its fluorescent fusion variant, ADPact-GFP, do not disrupt actin dynamics, ensuring accurate monitoring of cytoskeletal reorganization. Our findings provide a powerful tool for studying actin dynamics and offer fresh insights into the regulation of the cytoskeleton under physiological and pathological conditions.
肌动蛋白细胞骨架的动态组织对众多细胞过程至关重要,它受到肌动蛋白丝(F-肌动蛋白)的核苷酸状态的复杂调控。然而,用于特异性检测结合ADP的F-肌动蛋白的可视化工具仍然有限。在此,我们引入了ADPact,一种由20个氨基酸组成的肽,它能选择性地结合ADP-F-肌动蛋白。ADPact能够在体外和真核细胞中精确可视化ADP-F-肌动蛋白结构,尤其是在能量应激条件下,此时ADP-/ATP-肌动蛋白比率会增加。重要的是,ADPact及其荧光融合变体ADPact-GFP不会破坏肌动蛋白动力学,确保能够准确监测细胞骨架的重组。我们的研究结果为研究肌动蛋白动力学提供了一个强大的工具,并为生理和病理条件下细胞骨架的调控提供了新的见解。
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