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Fluorescent rhodamines and fluorogenic carbopyronines for super-resolution STED microscopy in living cells.

MPS-Authors
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Butkevich,  A.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Mitronova,  G.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Sidenstein,  S.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Klocke,  J.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Kamin,  D.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Meineke,  D. N. H.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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D'Este,  E.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Kraemer,  P. T.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Danzl,  J. G.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Belov,  V. N.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Hell,  S. W.
Department of NanoBiophotonics, MPI for Biophysical Chemistry, Max Planck Society;

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Fulltext (public)

2256448.pdf
(Publisher version), 4MB

Supplementary Material (public)

2256448_Suppl.pdf
(Supplementary material), 14MB

Citation

Butkevich, A., Mitronova, G., Sidenstein, S., Klocke, J., Kamin, D., Meineke, D. N. H., et al. (2016). Fluorescent rhodamines and fluorogenic carbopyronines for super-resolution STED microscopy in living cells. Angewandte Chemie International Edition, 55(10), 3290-3294. doi:10.1002/anie.201511018.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002A-041D-0
Abstract
A range of bright and photostable rhodamines and carbopyronines with absorption maxima in the range of λ=500-630 nm were prepared, and enabled the specific labeling of cytoskeletal filaments using HaloTag technology followed by staining with 1 μm solutions of the dye-ligand conjugates. The synthesis, photophysical parameters, fluorogenic behavior, and structure-property relationships of the new dyes are discussed. Light microscopy with stimulated emission depletion (STED) provided one- and two-color images of living cells with an optical resolution of 40-60 nm.