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Smart-aggregation imaging for single molecule localisation with SPAD cameras
Single molecule localisation microscopy (SMLM) has become an essential part of the super-resolution toolbox for probing cellular structure and function. The rapid evolution of these techniques has outstripped detector development and faster, more sensitive cameras are required to further improve loc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120354/ https://www.ncbi.nlm.nih.gov/pubmed/27876857 http://dx.doi.org/10.1038/srep37349 |
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author | Gyongy, Istvan Davies, Amy Dutton, Neale A. W. Duncan, Rory R. Rickman, Colin Henderson, Robert K. Dalgarno, Paul A. |
author_facet | Gyongy, Istvan Davies, Amy Dutton, Neale A. W. Duncan, Rory R. Rickman, Colin Henderson, Robert K. Dalgarno, Paul A. |
author_sort | Gyongy, Istvan |
collection | PubMed |
description | Single molecule localisation microscopy (SMLM) has become an essential part of the super-resolution toolbox for probing cellular structure and function. The rapid evolution of these techniques has outstripped detector development and faster, more sensitive cameras are required to further improve localisation certainty. Single-photon avalanche photodiode (SPAD) array cameras offer single-photon sensitivity, very high frame rates and zero readout noise, making them a potentially ideal detector for ultra-fast imaging and SMLM experiments. However, performance traditionally falls behind that of emCCD and sCMOS devices due to lower photon detection efficiency. Here we demonstrate, both experimentally and through simulations, that the sensitivity of a binary SPAD camera in SMLM experiments can be improved significantly by aggregating only frames containing signal, and that this leads to smaller datasets and competitive performance with that of existing detectors. The simulations also indicate that with predicted future advances in SPAD camera technology, SPAD devices will outperform existing scientific cameras when capturing fast temporal dynamics. |
format | Online Article Text |
id | pubmed-5120354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51203542016-11-28 Smart-aggregation imaging for single molecule localisation with SPAD cameras Gyongy, Istvan Davies, Amy Dutton, Neale A. W. Duncan, Rory R. Rickman, Colin Henderson, Robert K. Dalgarno, Paul A. Sci Rep Article Single molecule localisation microscopy (SMLM) has become an essential part of the super-resolution toolbox for probing cellular structure and function. The rapid evolution of these techniques has outstripped detector development and faster, more sensitive cameras are required to further improve localisation certainty. Single-photon avalanche photodiode (SPAD) array cameras offer single-photon sensitivity, very high frame rates and zero readout noise, making them a potentially ideal detector for ultra-fast imaging and SMLM experiments. However, performance traditionally falls behind that of emCCD and sCMOS devices due to lower photon detection efficiency. Here we demonstrate, both experimentally and through simulations, that the sensitivity of a binary SPAD camera in SMLM experiments can be improved significantly by aggregating only frames containing signal, and that this leads to smaller datasets and competitive performance with that of existing detectors. The simulations also indicate that with predicted future advances in SPAD camera technology, SPAD devices will outperform existing scientific cameras when capturing fast temporal dynamics. Nature Publishing Group 2016-11-23 /pmc/articles/PMC5120354/ /pubmed/27876857 http://dx.doi.org/10.1038/srep37349 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gyongy, Istvan Davies, Amy Dutton, Neale A. W. Duncan, Rory R. Rickman, Colin Henderson, Robert K. Dalgarno, Paul A. Smart-aggregation imaging for single molecule localisation with SPAD cameras |
title | Smart-aggregation imaging for single molecule localisation with SPAD cameras |
title_full | Smart-aggregation imaging for single molecule localisation with SPAD cameras |
title_fullStr | Smart-aggregation imaging for single molecule localisation with SPAD cameras |
title_full_unstemmed | Smart-aggregation imaging for single molecule localisation with SPAD cameras |
title_short | Smart-aggregation imaging for single molecule localisation with SPAD cameras |
title_sort | smart-aggregation imaging for single molecule localisation with spad cameras |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120354/ https://www.ncbi.nlm.nih.gov/pubmed/27876857 http://dx.doi.org/10.1038/srep37349 |
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