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Nat Commun ; 7: 10778, 2016 Mar 04.
Article in English | MEDLINE | ID: mdl-26940217

ABSTRACT

Stimulated emission depletion (STED) nanoscopy allows observations of subcellular dynamics at the nanoscale. Applications have, however, been severely limited by the lack of a versatile STED-compatible two-colour labelling strategy for intracellular targets in living cells. Here we demonstrate a universal labelling method based on the organic, membrane-permeable dyes SiR and ATTO590 as Halo and SNAP substrates. SiR and ATTO590 constitute the first suitable dye pair for two-colour STED imaging in living cells below 50 nm resolution. We show applications with mitochondria, endoplasmic reticulum, plasma membrane and Golgi-localized proteins, and demonstrate continuous acquisition for up to 3 min at 2-s time resolution.


Subject(s)
Heterocyclic Compounds, 4 or More Rings/chemistry , Luminescent Proteins , Microscopy, Fluorescence/methods , Nanotechnology/methods , Rhodamines/chemistry , Animals , COS Cells , Chlorocebus aethiops , HeLa Cells , Humans
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