A near-infrared fluorophore for live-cell super-resolution microscopy of cellular proteins

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Gražvydas Lukinavičius - , Swiss Federal Institute of Technology Lausanne (EPFL) (Author)
  • Keitaro Umezawa - , Swiss Federal Institute of Technology Lausanne (EPFL) (Author)
  • Nicolas Olivier - , Swiss Federal Institute of Technology Lausanne (EPFL) (Author)
  • Alf Honigmann - , Max Planck Institute for Biophysical Chemistry (Karl Friedrich Bonhoeffer Institute) (Author)
  • Guoying Yang - , European Molecular Biology Laboratory (EMBL) Monterotondo (Author)
  • Tilman Plass - , European Molecular Biology Laboratory (EMBL) Heidelberg (Author)
  • Veronika Mueller - , Max Planck Institute for Biophysical Chemistry (Karl Friedrich Bonhoeffer Institute) (Author)
  • Luc Reymond - , Swiss Federal Institute of Technology Lausanne (EPFL) (Author)
  • Ivan R. Corrêa - , New England Biolabs (Author)
  • Zhen Ge Luo - , CAS - Shanghai Institute of Nutrition and Health (Author)
  • Carsten Schultz - , European Molecular Biology Laboratory (EMBL) Heidelberg (Author)
  • Edward A. Lemke - , European Molecular Biology Laboratory (EMBL) Heidelberg (Author)
  • Paul Heppenstall - , European Molecular Biology Laboratory (EMBL) Monterotondo (Author)
  • Christian Eggeling - , Max Planck Institute for Biophysical Chemistry (Karl Friedrich Bonhoeffer Institute), University of Oxford (Author)
  • Suliana Manley - , Swiss Federal Institute of Technology Lausanne (EPFL) (Author)
  • Kai Johnsson - , Swiss Federal Institute of Technology Lausanne (EPFL) (Author)

Abstract

The ideal fluorescent probe for bioimaging is bright, absorbs at long wavelengths and can be implemented flexibly in living cells and in vivo. However, the design of synthetic fluorophores that combine all of these properties has proved to be extremely difficult. Here, we introduce a biocompatible near-infrared silicon-rhodamine probe that can be coupled specifically to proteins using different labelling techniques. Importantly, its high permeability and fluorogenic character permit the imaging of proteins in living cells and tissues, and its brightness and photostability make it ideally suited for live-cell super-resolution microscopy. The excellent spectroscopic properties of the probe combined with its ease of use in live-cell applications make it a powerful new tool for bioimaging.

Details

Original languageEnglish
Pages (from-to)132-139
Number of pages8
JournalNature chemistry
Volume5
Issue number2
Publication statusPublished - Feb 2013
Peer-reviewedYes
Externally publishedYes

External IDs

PubMed 23344448
ORCID /0000-0003-0475-3790/work/161889563

Keywords