Neuronal imaging with ultrahigh dynamic range multiphoton microscopy

Abstract Multiphoton microscopes are hampered by limited dynamic range, preventing weak sample features from being detected in the presence of strong features, or preventing the capture of unpredictable bursts in sample strength. We present a digital electronic add-on technique that vastly improves...

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Main Authors: Ruohui Yang, Timothy D. Weber, Ellen D. Witkowski, Ian G. Davison, Jerome Mertz
Format: Article
Language:English
Published: Nature Portfolio 2017-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-06065-7
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author Ruohui Yang
Timothy D. Weber
Ellen D. Witkowski
Ian G. Davison
Jerome Mertz
author_facet Ruohui Yang
Timothy D. Weber
Ellen D. Witkowski
Ian G. Davison
Jerome Mertz
author_sort Ruohui Yang
collection DOAJ
description Abstract Multiphoton microscopes are hampered by limited dynamic range, preventing weak sample features from being detected in the presence of strong features, or preventing the capture of unpredictable bursts in sample strength. We present a digital electronic add-on technique that vastly improves the dynamic range of a multiphoton microscope while limiting potential photodamage. The add-on provides real-time negative feedback to regulate the laser power delivered to the sample, and a log representation of the sample strength to accommodate ultrahigh dynamic range without loss of information. No microscope hardware modifications are required, making the technique readily compatible with commercial instruments. Benefits are shown in both structural and in-vivo functional mouse brain imaging applications.
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spelling doaj.art-418a4726ec0748a2a28bf1864c3ab0812022-12-21T18:33:04ZengNature PortfolioScientific Reports2045-23222017-07-01711710.1038/s41598-017-06065-7Neuronal imaging with ultrahigh dynamic range multiphoton microscopyRuohui Yang0Timothy D. Weber1Ellen D. Witkowski2Ian G. Davison3Jerome Mertz4Boston University Department of Biomedical EngineeringBoston University Department of Biomedical EngineeringBoston University Department of BiologyBoston University Department of BiologyBoston University Department of Biomedical EngineeringAbstract Multiphoton microscopes are hampered by limited dynamic range, preventing weak sample features from being detected in the presence of strong features, or preventing the capture of unpredictable bursts in sample strength. We present a digital electronic add-on technique that vastly improves the dynamic range of a multiphoton microscope while limiting potential photodamage. The add-on provides real-time negative feedback to regulate the laser power delivered to the sample, and a log representation of the sample strength to accommodate ultrahigh dynamic range without loss of information. No microscope hardware modifications are required, making the technique readily compatible with commercial instruments. Benefits are shown in both structural and in-vivo functional mouse brain imaging applications.https://doi.org/10.1038/s41598-017-06065-7
spellingShingle Ruohui Yang
Timothy D. Weber
Ellen D. Witkowski
Ian G. Davison
Jerome Mertz
Neuronal imaging with ultrahigh dynamic range multiphoton microscopy
Scientific Reports
title Neuronal imaging with ultrahigh dynamic range multiphoton microscopy
title_full Neuronal imaging with ultrahigh dynamic range multiphoton microscopy
title_fullStr Neuronal imaging with ultrahigh dynamic range multiphoton microscopy
title_full_unstemmed Neuronal imaging with ultrahigh dynamic range multiphoton microscopy
title_short Neuronal imaging with ultrahigh dynamic range multiphoton microscopy
title_sort neuronal imaging with ultrahigh dynamic range multiphoton microscopy
url https://doi.org/10.1038/s41598-017-06065-7
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AT timothydweber neuronalimagingwithultrahighdynamicrangemultiphotonmicroscopy
AT ellendwitkowski neuronalimagingwithultrahighdynamicrangemultiphotonmicroscopy
AT iangdavison neuronalimagingwithultrahighdynamicrangemultiphotonmicroscopy
AT jeromemertz neuronalimagingwithultrahighdynamicrangemultiphotonmicroscopy