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Ultra-High Resolution 3D Imaging of Whole Cells
Fluorescence nanoscopy, or super-resolution microscopy, has become an important tool in cell biological research. However, because of its usually inferior resolution in the depth direction (50–80 nm) and rapidly deteriorating resolution in thick samples, its practical biological application has been...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005454/ https://www.ncbi.nlm.nih.gov/pubmed/27397506 http://dx.doi.org/10.1016/j.cell.2016.06.016 |
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author | Huang, Fang Sirinakis, George Allgeyer, Edward S. Schroeder, Lena K. Duim, Whitney C. Kromann, Emil B. Phan, Thomy Rivera-Molina, Felix E. Myers, Jordan R. Irnov, Irnov Lessard, Mark Zhang, Yongdeng Handel, Mary Ann Jacobs-Wagner, Christine Lusk, C. Patrick Rothman, James E. Toomre, Derek Booth, Martin J. Bewersdorf, Joerg |
author_facet | Huang, Fang Sirinakis, George Allgeyer, Edward S. Schroeder, Lena K. Duim, Whitney C. Kromann, Emil B. Phan, Thomy Rivera-Molina, Felix E. Myers, Jordan R. Irnov, Irnov Lessard, Mark Zhang, Yongdeng Handel, Mary Ann Jacobs-Wagner, Christine Lusk, C. Patrick Rothman, James E. Toomre, Derek Booth, Martin J. Bewersdorf, Joerg |
author_sort | Huang, Fang |
collection | PubMed |
description | Fluorescence nanoscopy, or super-resolution microscopy, has become an important tool in cell biological research. However, because of its usually inferior resolution in the depth direction (50–80 nm) and rapidly deteriorating resolution in thick samples, its practical biological application has been effectively limited to two dimensions and thin samples. Here, we present the development of whole-cell 4Pi single-molecule switching nanoscopy (W-4PiSMSN), an optical nanoscope that allows imaging of three-dimensional (3D) structures at 10- to 20-nm resolution throughout entire mammalian cells. We demonstrate the wide applicability of W-4PiSMSN across diverse research fields by imaging complex molecular architectures ranging from bacteriophages to nuclear pores, cilia, and synaptonemal complexes in large 3D cellular volumes. |
format | Online Article Text |
id | pubmed-5005454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50054542016-09-01 Ultra-High Resolution 3D Imaging of Whole Cells Huang, Fang Sirinakis, George Allgeyer, Edward S. Schroeder, Lena K. Duim, Whitney C. Kromann, Emil B. Phan, Thomy Rivera-Molina, Felix E. Myers, Jordan R. Irnov, Irnov Lessard, Mark Zhang, Yongdeng Handel, Mary Ann Jacobs-Wagner, Christine Lusk, C. Patrick Rothman, James E. Toomre, Derek Booth, Martin J. Bewersdorf, Joerg Cell Resource Fluorescence nanoscopy, or super-resolution microscopy, has become an important tool in cell biological research. However, because of its usually inferior resolution in the depth direction (50–80 nm) and rapidly deteriorating resolution in thick samples, its practical biological application has been effectively limited to two dimensions and thin samples. Here, we present the development of whole-cell 4Pi single-molecule switching nanoscopy (W-4PiSMSN), an optical nanoscope that allows imaging of three-dimensional (3D) structures at 10- to 20-nm resolution throughout entire mammalian cells. We demonstrate the wide applicability of W-4PiSMSN across diverse research fields by imaging complex molecular architectures ranging from bacteriophages to nuclear pores, cilia, and synaptonemal complexes in large 3D cellular volumes. Cell Press 2016-08-11 /pmc/articles/PMC5005454/ /pubmed/27397506 http://dx.doi.org/10.1016/j.cell.2016.06.016 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Resource Huang, Fang Sirinakis, George Allgeyer, Edward S. Schroeder, Lena K. Duim, Whitney C. Kromann, Emil B. Phan, Thomy Rivera-Molina, Felix E. Myers, Jordan R. Irnov, Irnov Lessard, Mark Zhang, Yongdeng Handel, Mary Ann Jacobs-Wagner, Christine Lusk, C. Patrick Rothman, James E. Toomre, Derek Booth, Martin J. Bewersdorf, Joerg Ultra-High Resolution 3D Imaging of Whole Cells |
title | Ultra-High Resolution 3D Imaging of Whole Cells |
title_full | Ultra-High Resolution 3D Imaging of Whole Cells |
title_fullStr | Ultra-High Resolution 3D Imaging of Whole Cells |
title_full_unstemmed | Ultra-High Resolution 3D Imaging of Whole Cells |
title_short | Ultra-High Resolution 3D Imaging of Whole Cells |
title_sort | ultra-high resolution 3d imaging of whole cells |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005454/ https://www.ncbi.nlm.nih.gov/pubmed/27397506 http://dx.doi.org/10.1016/j.cell.2016.06.016 |
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