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Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging
Super‐resolution fluorescence imaging provides critically improved information about the composition, organization, and dynamics of subcellular structures. Quantum dot triexciton imaging (QDTI) has been introduced as an easy‐to‐use sub‐diffraction imaging method that achieves an almost 2‐fold improv...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634860/ https://www.ncbi.nlm.nih.gov/pubmed/34228908 http://dx.doi.org/10.1002/2211-5463.13246 |
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author | Hennig, Simon Manstein, Dietmar J. |
author_facet | Hennig, Simon Manstein, Dietmar J. |
author_sort | Hennig, Simon |
collection | PubMed |
description | Super‐resolution fluorescence imaging provides critically improved information about the composition, organization, and dynamics of subcellular structures. Quantum dot triexciton imaging (QDTI) has been introduced as an easy‐to‐use sub‐diffraction imaging method that achieves an almost 2‐fold improvement in resolution when used with conventional confocal microscopes. Here, we report an overall 3‐fold increase in lateral and axial resolution compared to conventional confocal microscopes by combining QDTI with state‐of‐the‐art commercial laser scanning microscope systems. |
format | Online Article Text |
id | pubmed-8634860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86348602021-12-08 Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging Hennig, Simon Manstein, Dietmar J. FEBS Open Bio Method Super‐resolution fluorescence imaging provides critically improved information about the composition, organization, and dynamics of subcellular structures. Quantum dot triexciton imaging (QDTI) has been introduced as an easy‐to‐use sub‐diffraction imaging method that achieves an almost 2‐fold improvement in resolution when used with conventional confocal microscopes. Here, we report an overall 3‐fold increase in lateral and axial resolution compared to conventional confocal microscopes by combining QDTI with state‐of‐the‐art commercial laser scanning microscope systems. John Wiley and Sons Inc. 2021-07-26 /pmc/articles/PMC8634860/ /pubmed/34228908 http://dx.doi.org/10.1002/2211-5463.13246 Text en © 2021 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Method Hennig, Simon Manstein, Dietmar J. Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
title | Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
title_full | Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
title_fullStr | Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
title_full_unstemmed | Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
title_short | Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
title_sort | improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634860/ https://www.ncbi.nlm.nih.gov/pubmed/34228908 http://dx.doi.org/10.1002/2211-5463.13246 |
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