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High density three-dimensional localization microscopy across large volumes
Extending three-dimensional (3D) single molecule localization microscopy away from the coverslip and into thicker specimens will greatly broaden its biological utility. However, localizing molecules in 3D with high precision in such samples, while simultaneously achieving the extreme labeling densit...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889433/ https://www.ncbi.nlm.nih.gov/pubmed/26950745 http://dx.doi.org/10.1038/nmeth.3797 |
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author | Legant, Wesley R. Shao, Lin Grimm, Jonathan B. Brown, Timothy A. Milkie, Daniel E. Avants, Brian B. Lavis, Luke D. Betzig, Eric |
author_facet | Legant, Wesley R. Shao, Lin Grimm, Jonathan B. Brown, Timothy A. Milkie, Daniel E. Avants, Brian B. Lavis, Luke D. Betzig, Eric |
author_sort | Legant, Wesley R. |
collection | PubMed |
description | Extending three-dimensional (3D) single molecule localization microscopy away from the coverslip and into thicker specimens will greatly broaden its biological utility. However, localizing molecules in 3D with high precision in such samples, while simultaneously achieving the extreme labeling densities required for high resolution of densely crowded structures is challenging due to the limitations both of conventional imaging modalities and of conventional labeling techniques. Here, we combine lattice light sheet microscopy with newly developed, freely diffusing, cell permeable chemical probes with targeted affinity towards either DNA, intracellular membranes, or the plasma membrane. We use this combination to perform high localization precision, ultra-high labeling density, multicolor localization microscopy in samples up to 20 microns thick, including dividing cells and the neuromast organ of a zebrafish embryo. We also demonstrate super-resolution correlative imaging with protein specific photoactivable fluorophores, providing a mutually compatible, single platform alternative to correlative light-electron microscopy over large volumes. |
format | Online Article Text |
id | pubmed-4889433 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-48894332016-09-07 High density three-dimensional localization microscopy across large volumes Legant, Wesley R. Shao, Lin Grimm, Jonathan B. Brown, Timothy A. Milkie, Daniel E. Avants, Brian B. Lavis, Luke D. Betzig, Eric Nat Methods Article Extending three-dimensional (3D) single molecule localization microscopy away from the coverslip and into thicker specimens will greatly broaden its biological utility. However, localizing molecules in 3D with high precision in such samples, while simultaneously achieving the extreme labeling densities required for high resolution of densely crowded structures is challenging due to the limitations both of conventional imaging modalities and of conventional labeling techniques. Here, we combine lattice light sheet microscopy with newly developed, freely diffusing, cell permeable chemical probes with targeted affinity towards either DNA, intracellular membranes, or the plasma membrane. We use this combination to perform high localization precision, ultra-high labeling density, multicolor localization microscopy in samples up to 20 microns thick, including dividing cells and the neuromast organ of a zebrafish embryo. We also demonstrate super-resolution correlative imaging with protein specific photoactivable fluorophores, providing a mutually compatible, single platform alternative to correlative light-electron microscopy over large volumes. 2016-03-07 2016-04 /pmc/articles/PMC4889433/ /pubmed/26950745 http://dx.doi.org/10.1038/nmeth.3797 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Legant, Wesley R. Shao, Lin Grimm, Jonathan B. Brown, Timothy A. Milkie, Daniel E. Avants, Brian B. Lavis, Luke D. Betzig, Eric High density three-dimensional localization microscopy across large volumes |
title | High density three-dimensional localization microscopy across large volumes |
title_full | High density three-dimensional localization microscopy across large volumes |
title_fullStr | High density three-dimensional localization microscopy across large volumes |
title_full_unstemmed | High density three-dimensional localization microscopy across large volumes |
title_short | High density three-dimensional localization microscopy across large volumes |
title_sort | high density three-dimensional localization microscopy across large volumes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889433/ https://www.ncbi.nlm.nih.gov/pubmed/26950745 http://dx.doi.org/10.1038/nmeth.3797 |
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