Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors

Abstract Genetically encoded biosensors function by linking structural change in a protein construct, typically tagged with one or more fluorescent proteins, to changes in a biological parameter of interest (such as calcium concentration, pH, phosphorylation-state, etc.). Typically, the structural c...

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Main Authors: Tuan A. Nguyen, Henry L. Puhl, An K. Pham, Steven S. Vogel
Format: Article
Language:English
Published: Nature Publishing Group 2018-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-25689-x
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spelling doaj-2325b19a934c460e9d076cd0bad586232020-12-08T06:25:19ZengNature Publishing GroupScientific Reports2045-23222018-05-018111710.1038/s41598-018-25689-xAuto-FPFA: An Automated Microscope for Characterizing Genetically Encoded BiosensorsTuan A. Nguyen0Henry L. Puhl1An K. Pham2Steven S. Vogel3Laboratory of Molecular Physiology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of HealthLaboratory of Molecular Physiology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of HealthLaboratory of Molecular Physiology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of HealthLaboratory of Molecular Physiology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of HealthAbstract Genetically encoded biosensors function by linking structural change in a protein construct, typically tagged with one or more fluorescent proteins, to changes in a biological parameter of interest (such as calcium concentration, pH, phosphorylation-state, etc.). Typically, the structural change triggered by alterations in the bio-parameter is monitored as a change in either fluorescent intensity, or lifetime. Potentially, other photo-physical properties of fluorophores, such as fluorescence anisotropy, molecular brightness, concentration, and lateral and/or rotational diffusion could also be used. Furthermore, while it is likely that multiple photo-physical attributes of a biosensor might be altered as a function of the bio-parameter, standard measurements monitor only a single photo-physical trait. This limits how biosensors are designed, as well as the accuracy and interpretation of biosensor measurements. Here we describe the design and construction of an automated multimodal-microscope. This system can autonomously analyze 96 samples in a micro-titer dish and for each sample simultaneously measure intensity (photon count), fluorescence lifetime, time-resolved anisotropy, molecular brightness, lateral diffusion time, and concentration. We characterize the accuracy and precision of this instrument, and then demonstrate its utility by characterizing three types of genetically encoded calcium sensors as well as a negative control.https://doi.org/10.1038/s41598-018-25689-x
collection DOAJ
language English
format Article
sources DOAJ
author Tuan A. Nguyen
Henry L. Puhl
An K. Pham
Steven S. Vogel
spellingShingle Tuan A. Nguyen
Henry L. Puhl
An K. Pham
Steven S. Vogel
Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors
Scientific Reports
author_facet Tuan A. Nguyen
Henry L. Puhl
An K. Pham
Steven S. Vogel
author_sort Tuan A. Nguyen
title Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors
title_short Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors
title_full Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors
title_fullStr Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors
title_full_unstemmed Auto-FPFA: An Automated Microscope for Characterizing Genetically Encoded Biosensors
title_sort auto-fpfa: an automated microscope for characterizing genetically encoded biosensors
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-05-01
description Abstract Genetically encoded biosensors function by linking structural change in a protein construct, typically tagged with one or more fluorescent proteins, to changes in a biological parameter of interest (such as calcium concentration, pH, phosphorylation-state, etc.). Typically, the structural change triggered by alterations in the bio-parameter is monitored as a change in either fluorescent intensity, or lifetime. Potentially, other photo-physical properties of fluorophores, such as fluorescence anisotropy, molecular brightness, concentration, and lateral and/or rotational diffusion could also be used. Furthermore, while it is likely that multiple photo-physical attributes of a biosensor might be altered as a function of the bio-parameter, standard measurements monitor only a single photo-physical trait. This limits how biosensors are designed, as well as the accuracy and interpretation of biosensor measurements. Here we describe the design and construction of an automated multimodal-microscope. This system can autonomously analyze 96 samples in a micro-titer dish and for each sample simultaneously measure intensity (photon count), fluorescence lifetime, time-resolved anisotropy, molecular brightness, lateral diffusion time, and concentration. We characterize the accuracy and precision of this instrument, and then demonstrate its utility by characterizing three types of genetically encoded calcium sensors as well as a negative control.
url https://doi.org/10.1038/s41598-018-25689-x
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