荧光
荧光团
化学
肌动蛋白
活体细胞成像
生物物理学
扫描电镜
动力学(音乐)
荧光显微镜
踏步
肌动蛋白结合蛋白
细胞生物学
荧光寿命成像显微镜
聚合
纳米技术
微丝
肌动蛋白重塑
肌动蛋白细胞骨架
作者
Veselin Nasufović,Julian Kompa,Halli L. Lindamood,Merle Blümke,Rayane Dibsy,Birgit Koch,Victoria Levario‐Diaz,Katharina Weber,Marlene Maager,Ekaterina Nomerotskaia,Arnaud Échard,Elisabetta Ada Cavalcanti‐Adam,Eric A. Vitriol,Hans‐Dieter Arndt,Kai Johnsson
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-16
卷期号:64 (50): e202509285-e202509285
被引量:1
标识
DOI:10.1002/anie.202509285
摘要
Imaging actin-dependent processes in live cells is important for understanding numerous biological processes. However, currently used natural-product-based fluorescent probes for actin filaments affect the dynamics of actin polymerization and can induce undesired cellular phenotypes. Here, we introduce SiR-XActin, a simplified jasplakinolide-based, far-red fluorescent probe that enables bright and photostable staining in various cell types without requiring genetic modifications. Due to its relatively weak binding affinity, the probe exhibits minimal cytotoxicity and labels actin filaments without significantly altering actin dynamics. Furthermore, SiR-XActin is suitable for time-resolved, live-cell super-resolution STED microscopy. Exchanging the SiR fluorophore in SiR-XActin for other fluorophores yields probes in different colors. All these properties make SiR-XActin and its analogs powerful tools for studying actin dynamics using live-cell fluorescence microscopy.
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