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Small-Molecule Labeling of Live Cell Surfaces for Three-Dimensional Super-Resolution Microscopy
[Image: see text] Precise imaging of the cell surface of fluorescently labeled bacteria requires super-resolution methods because the size-scale of these cells is on the order of the diffraction limit. In this work, we present a photocontrollable small-molecule rhodamine spirolactam emitter suitable...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195381/ https://www.ncbi.nlm.nih.gov/pubmed/25222297 http://dx.doi.org/10.1021/ja508028h |
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author | Lee, Marissa K. Rai, Prabin Williams, Jarrod Twieg, Robert J. Moerner, W. E. |
author_facet | Lee, Marissa K. Rai, Prabin Williams, Jarrod Twieg, Robert J. Moerner, W. E. |
author_sort | Lee, Marissa K. |
collection | PubMed |
description | [Image: see text] Precise imaging of the cell surface of fluorescently labeled bacteria requires super-resolution methods because the size-scale of these cells is on the order of the diffraction limit. In this work, we present a photocontrollable small-molecule rhodamine spirolactam emitter suitable for non-toxic and specific labeling of the outer surface of cells for three-dimensional (3D) super-resolution (SR) imaging. Conventional rhodamine spirolactams photoswitch to the emitting form with UV light; however, these wavelengths can damage cells. We extended photoswitching to visible wavelengths >400 nm by iterative synthesis and spectroscopic characterization to optimize the substitution on the spirolactam. Further, an N-hydroxysuccinimide-functionalized derivative enabled covalent labeling of amines on the surface of live Caulobacter crescentus cells. Resulting 3D SR reconstructions of the labeled cell surface reveal uniform and specific sampling with thousands of localizations per cell and excellent localization precision in x, y, and z. The distribution of cell stalk lengths (a sub-diffraction-sized cellular structure) was quantified for a mixed population of cells. Pulse-chase experiments identified sites of cell surface growth. Covalent labeling with the optimized rhodamine spirolactam label provides a general strategy to study the surfaces of living cells with high specificity and resolution down to 10–20 nm. |
format | Online Article Text |
id | pubmed-4195381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41953812015-09-15 Small-Molecule Labeling of Live Cell Surfaces for Three-Dimensional Super-Resolution Microscopy Lee, Marissa K. Rai, Prabin Williams, Jarrod Twieg, Robert J. Moerner, W. E. J Am Chem Soc [Image: see text] Precise imaging of the cell surface of fluorescently labeled bacteria requires super-resolution methods because the size-scale of these cells is on the order of the diffraction limit. In this work, we present a photocontrollable small-molecule rhodamine spirolactam emitter suitable for non-toxic and specific labeling of the outer surface of cells for three-dimensional (3D) super-resolution (SR) imaging. Conventional rhodamine spirolactams photoswitch to the emitting form with UV light; however, these wavelengths can damage cells. We extended photoswitching to visible wavelengths >400 nm by iterative synthesis and spectroscopic characterization to optimize the substitution on the spirolactam. Further, an N-hydroxysuccinimide-functionalized derivative enabled covalent labeling of amines on the surface of live Caulobacter crescentus cells. Resulting 3D SR reconstructions of the labeled cell surface reveal uniform and specific sampling with thousands of localizations per cell and excellent localization precision in x, y, and z. The distribution of cell stalk lengths (a sub-diffraction-sized cellular structure) was quantified for a mixed population of cells. Pulse-chase experiments identified sites of cell surface growth. Covalent labeling with the optimized rhodamine spirolactam label provides a general strategy to study the surfaces of living cells with high specificity and resolution down to 10–20 nm. American Chemical Society 2014-09-15 2014-10-08 /pmc/articles/PMC4195381/ /pubmed/25222297 http://dx.doi.org/10.1021/ja508028h Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Lee, Marissa K. Rai, Prabin Williams, Jarrod Twieg, Robert J. Moerner, W. E. Small-Molecule Labeling of Live Cell Surfaces for Three-Dimensional Super-Resolution Microscopy |
title | Small-Molecule
Labeling of Live Cell Surfaces for
Three-Dimensional Super-Resolution Microscopy |
title_full | Small-Molecule
Labeling of Live Cell Surfaces for
Three-Dimensional Super-Resolution Microscopy |
title_fullStr | Small-Molecule
Labeling of Live Cell Surfaces for
Three-Dimensional Super-Resolution Microscopy |
title_full_unstemmed | Small-Molecule
Labeling of Live Cell Surfaces for
Three-Dimensional Super-Resolution Microscopy |
title_short | Small-Molecule
Labeling of Live Cell Surfaces for
Three-Dimensional Super-Resolution Microscopy |
title_sort | small-molecule
labeling of live cell surfaces for
three-dimensional super-resolution microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4195381/ https://www.ncbi.nlm.nih.gov/pubmed/25222297 http://dx.doi.org/10.1021/ja508028h |
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