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PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors
Genetically encoded ratiometric fluorescent probes are cutting-edge tools in biology. They allow precise and dynamic measurement of various physiological parameters within cell compartments. Because data extraction and analysis are time consuming and may lead to inconsistencies between results, we d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486618/ https://www.ncbi.nlm.nih.gov/pubmed/32953466 http://dx.doi.org/10.1016/j.mex.2020.101034 |
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author | Lévy, Elise Jaffrézic, Florence Laloë, Denis Rezaei, Human Huang, Meng-Er Béringue, Vincent Martin, Davy Vernis, Laurence |
author_facet | Lévy, Elise Jaffrézic, Florence Laloë, Denis Rezaei, Human Huang, Meng-Er Béringue, Vincent Martin, Davy Vernis, Laurence |
author_sort | Lévy, Elise |
collection | PubMed |
description | Genetically encoded ratiometric fluorescent probes are cutting-edge tools in biology. They allow precise and dynamic measurement of various physiological parameters within cell compartments. Because data extraction and analysis are time consuming and may lead to inconsistencies between results, we describe here a standardized pipeline for: • Semi-automated treatment of time-lapse fluorescence microscopy images. • Quantification of individual cell signal. • Statistical analysis of the data. First, a dedicated macro was developed using the FIJI software to reproducibly quantify the fluorescence ratio as a function of time. Raw data are then exported and analyzed using R and MATLAB softwares. Calculation and statistical analysis of selected graphic parameters are performed. In addition, a functional principal component analysis allows summarizing the dataset. Finally, a principal component analysis is performed to check consistency and final analysis is presented as a visual diagram. The method is adapted to any ratiometric fluorescent probe. As an example, the analysis of the cytoplasmic HyPer probe in response to an acute cell treatment with increasing amounts of hydrogen peroxide is shown. In conclusion, the pipeline allows to save time and analyze a larger amount of samples while reducing manual interventions and consequently increasing the robustness of the analysis. |
format | Online Article Text |
id | pubmed-7486618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74866182020-09-18 PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors Lévy, Elise Jaffrézic, Florence Laloë, Denis Rezaei, Human Huang, Meng-Er Béringue, Vincent Martin, Davy Vernis, Laurence MethodsX Method Article Genetically encoded ratiometric fluorescent probes are cutting-edge tools in biology. They allow precise and dynamic measurement of various physiological parameters within cell compartments. Because data extraction and analysis are time consuming and may lead to inconsistencies between results, we describe here a standardized pipeline for: • Semi-automated treatment of time-lapse fluorescence microscopy images. • Quantification of individual cell signal. • Statistical analysis of the data. First, a dedicated macro was developed using the FIJI software to reproducibly quantify the fluorescence ratio as a function of time. Raw data are then exported and analyzed using R and MATLAB softwares. Calculation and statistical analysis of selected graphic parameters are performed. In addition, a functional principal component analysis allows summarizing the dataset. Finally, a principal component analysis is performed to check consistency and final analysis is presented as a visual diagram. The method is adapted to any ratiometric fluorescent probe. As an example, the analysis of the cytoplasmic HyPer probe in response to an acute cell treatment with increasing amounts of hydrogen peroxide is shown. In conclusion, the pipeline allows to save time and analyze a larger amount of samples while reducing manual interventions and consequently increasing the robustness of the analysis. Elsevier 2020-08-26 /pmc/articles/PMC7486618/ /pubmed/32953466 http://dx.doi.org/10.1016/j.mex.2020.101034 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Method Article Lévy, Elise Jaffrézic, Florence Laloë, Denis Rezaei, Human Huang, Meng-Er Béringue, Vincent Martin, Davy Vernis, Laurence PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
title | PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
title_full | PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
title_fullStr | PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
title_full_unstemmed | PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
title_short | PiQSARS: A pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
title_sort | piqsars: a pipeline for quantitative and statistical analyses of ratiometric fluorescent biosensors |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486618/ https://www.ncbi.nlm.nih.gov/pubmed/32953466 http://dx.doi.org/10.1016/j.mex.2020.101034 |
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