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SiR-XActin: A Fluorescent Probe for Imaging Actin Dynamics in Live Cells

  • Veselin Nasufovic
  • , Julian Kompa
  • , Halli L. Lindamood
  • , Merle Blümke
  • , Rayane Dibsy
  • , Birgit Koch
  • , Victoria Levario-Diaz
  • , Katharina Weber
  • , Marlene Maager
  • , Ekaterina Nomerotskaia
  • , Arnaud Echard
  • , Elisabetta Ada Cavalcanti-Adam
  • , Eric A. Vitriol
  • , Hans Dieter Arndt
  • , Kai Johnsson
  • Friedrich-Schiller University
  • Max Planck Institute for Medical Research
  • Medical College of Georgia
  • Laboratoire de Probabilités et Modèles Aléatoires
  • University of Bayreuth
  • École Polytechnique

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Article numbere202509285
JournalAngewandte Chemie - International Edition
Volume64
Issue number50
DOIs
Publication statusPublished - 8 Dec 2025
Externally publishedYes

Keywords

  • F-actin
  • Fluorescent probes
  • Jasplakinolide derivatives
  • No-wash live-cell imaging
  • STED microscopy

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