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Cega: a single particle segmentation algorithm to identify moving particles in a noisy system
Improvements to particle tracking algorithms are required to effectively analyze the motility of biological molecules in complex or noisy systems. A typical single particle tracking (SPT) algorithm detects particle coordinates for trajectory assembly. However, particle detection filters fail for dat...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108521/ https://www.ncbi.nlm.nih.gov/pubmed/33788586 http://dx.doi.org/10.1091/mbc.E20-11-0744 |
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author | Masucci, Erin M. Relich, Peter K. Ostap, E. Michael Holzbaur, Erika L. F. Lakadamyali, Melike |
author_facet | Masucci, Erin M. Relich, Peter K. Ostap, E. Michael Holzbaur, Erika L. F. Lakadamyali, Melike |
author_sort | Masucci, Erin M. |
collection | PubMed |
description | Improvements to particle tracking algorithms are required to effectively analyze the motility of biological molecules in complex or noisy systems. A typical single particle tracking (SPT) algorithm detects particle coordinates for trajectory assembly. However, particle detection filters fail for data sets with low signal-to-noise levels. When tracking molecular motors in complex systems, standard techniques often fail to separate the fluorescent signatures of moving particles from background signal. We developed an approach to analyze the motility of kinesin motor proteins moving along the microtubule cytoskeleton of extracted neurons using the Kullback-Leibler divergence to identify regions where there are significant differences between models of moving particles and background signal. We tested our software on both simulated and experimental data and found a noticeable improvement in SPT capability and a higher identification rate of motors as compared with current methods. This algorithm, called Cega, for “find the object,” produces data amenable to conventional blob detection techniques that can then be used to obtain coordinates for downstream SPT processing. We anticipate that this algorithm will be useful for those interested in tracking moving particles in complex in vitro or in vivo environments. |
format | Online Article Text |
id | pubmed-8108521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-81085212021-07-04 Cega: a single particle segmentation algorithm to identify moving particles in a noisy system Masucci, Erin M. Relich, Peter K. Ostap, E. Michael Holzbaur, Erika L. F. Lakadamyali, Melike Mol Biol Cell Articles Improvements to particle tracking algorithms are required to effectively analyze the motility of biological molecules in complex or noisy systems. A typical single particle tracking (SPT) algorithm detects particle coordinates for trajectory assembly. However, particle detection filters fail for data sets with low signal-to-noise levels. When tracking molecular motors in complex systems, standard techniques often fail to separate the fluorescent signatures of moving particles from background signal. We developed an approach to analyze the motility of kinesin motor proteins moving along the microtubule cytoskeleton of extracted neurons using the Kullback-Leibler divergence to identify regions where there are significant differences between models of moving particles and background signal. We tested our software on both simulated and experimental data and found a noticeable improvement in SPT capability and a higher identification rate of motors as compared with current methods. This algorithm, called Cega, for “find the object,” produces data amenable to conventional blob detection techniques that can then be used to obtain coordinates for downstream SPT processing. We anticipate that this algorithm will be useful for those interested in tracking moving particles in complex in vitro or in vivo environments. The American Society for Cell Biology 2021-04-19 /pmc/articles/PMC8108521/ /pubmed/33788586 http://dx.doi.org/10.1091/mbc.E20-11-0744 Text en © 2021 Masucci et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/3.0/This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Masucci, Erin M. Relich, Peter K. Ostap, E. Michael Holzbaur, Erika L. F. Lakadamyali, Melike Cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
title | Cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
title_full | Cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
title_fullStr | Cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
title_full_unstemmed | Cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
title_short | Cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
title_sort | cega: a single particle segmentation algorithm to identify moving particles in a noisy system |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108521/ https://www.ncbi.nlm.nih.gov/pubmed/33788586 http://dx.doi.org/10.1091/mbc.E20-11-0744 |
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