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

  • Gražvydas Lukinavičius
  • , Keitaro Umezawa
  • , Nicolas Olivier
  • , Alf Honigmann
  • , Guoying Yang
  • , Tilman Plass
  • , Veronika Mueller
  • , Luc Reymond
  • , Ivan R. Corrêa
  • , Zhen Ge Luo
  • , Carsten Schultz
  • , Edward A. Lemke
  • , Paul Heppenstall
  • , Christian Eggeling
  • , Suliana Manley
  • , Kai Johnsson
  • ENAC-IIC-GEL
  • Biochemistry of Signal Dynamics
  • European Molecular Biology Laboratory Monterotondo
  • European Molecular Biology Laboratory Heidelberg
  • New England Biolabs
  • Shanghai Institute of Nutrition and Health
  • NDM

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

Résumé

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.

langue originaleAnglais
Pages (de - à)132-139
Nombre de pages8
journalNature Chemistry
Volume5
Numéro de publication2
Les DOIs
étatPublié - 1 févr. 2013
Modification externeOui

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