Folate Measurement in Mammalian Tissues by Fluorescence Polarization

Measurement of folate in animal tissues is expensive and time-consuming. A fluorescence polarization assay has been developed that allows the rapid and inexpensive quantification of folate in various animal tissues. The concentration of tissue folate is determined by its ability to compete with the...

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Main Authors: Harry Martin, Comeskey Daniel
Format: Article
Language:English
Published: De Gruyter 2011-02-01
Series:Pteridines
Subjects:
Online Access:https://doi.org/10.1515/pteridines.2011.22.1.105
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spelling doaj-001f908ebc1a48a6849b04dd165f98352021-09-05T14:00:03ZengDe GruyterPteridines0933-48072195-47202011-02-0122110511010.1515/pteridines.2011.22.1.105Folate Measurement in Mammalian Tissues by Fluorescence PolarizationHarry Martin0Comeskey Daniel1New Zealand Institute for Plant and Food Research, Tennant Drive, 4442 Palmerston North, Tel.:+64 6 953 7747, FAX.:+64 6 351 7050James Starley Building, Faculty of Health and Life Sciences, Coventry University, Coventry CV1 5FB, UKMeasurement of folate in animal tissues is expensive and time-consuming. A fluorescence polarization assay has been developed that allows the rapid and inexpensive quantification of folate in various animal tissues. The concentration of tissue folate is determined by its ability to compete with the binding of Alexa-660-folate to bovine milk folate binding protein. The technique uses a few milligrams of material and is amenable to automated screening in 384-well microplates. Using this approach, the folate concentration in mouse liver, kidney & brain was found to be 21.4, 4.22 and 0.73 nanomoles/g fresh tissue, respectively. Packed human erythrocytes were found to contain 1.31 mM folate. These estimates are similar to published folate values for these tissues. Ascorbate was not included in the assay buffer because of its pro-oxidant effects in iron rich tissues such as erythrocytes and liver. The assay is homogeneous, completed within a few hours of the availability of the samples, and will enable the high throughput analyses of folate in human and animal samples.https://doi.org/10.1515/pteridines.2011.22.1.105folate assayfluorescence polarizationfolate binding proteinalexa-fluor-660erythrocyteliverbrainkidney
collection DOAJ
language English
format Article
sources DOAJ
author Harry Martin
Comeskey Daniel
spellingShingle Harry Martin
Comeskey Daniel
Folate Measurement in Mammalian Tissues by Fluorescence Polarization
Pteridines
folate assay
fluorescence polarization
folate binding protein
alexa-fluor-660
erythrocyte
liver
brain
kidney
author_facet Harry Martin
Comeskey Daniel
author_sort Harry Martin
title Folate Measurement in Mammalian Tissues by Fluorescence Polarization
title_short Folate Measurement in Mammalian Tissues by Fluorescence Polarization
title_full Folate Measurement in Mammalian Tissues by Fluorescence Polarization
title_fullStr Folate Measurement in Mammalian Tissues by Fluorescence Polarization
title_full_unstemmed Folate Measurement in Mammalian Tissues by Fluorescence Polarization
title_sort folate measurement in mammalian tissues by fluorescence polarization
publisher De Gruyter
series Pteridines
issn 0933-4807
2195-4720
publishDate 2011-02-01
description Measurement of folate in animal tissues is expensive and time-consuming. A fluorescence polarization assay has been developed that allows the rapid and inexpensive quantification of folate in various animal tissues. The concentration of tissue folate is determined by its ability to compete with the binding of Alexa-660-folate to bovine milk folate binding protein. The technique uses a few milligrams of material and is amenable to automated screening in 384-well microplates. Using this approach, the folate concentration in mouse liver, kidney & brain was found to be 21.4, 4.22 and 0.73 nanomoles/g fresh tissue, respectively. Packed human erythrocytes were found to contain 1.31 mM folate. These estimates are similar to published folate values for these tissues. Ascorbate was not included in the assay buffer because of its pro-oxidant effects in iron rich tissues such as erythrocytes and liver. The assay is homogeneous, completed within a few hours of the availability of the samples, and will enable the high throughput analyses of folate in human and animal samples.
topic folate assay
fluorescence polarization
folate binding protein
alexa-fluor-660
erythrocyte
liver
brain
kidney
url https://doi.org/10.1515/pteridines.2011.22.1.105
work_keys_str_mv AT harrymartin folatemeasurementinmammaliantissuesbyfluorescencepolarization
AT comeskeydaniel folatemeasurementinmammaliantissuesbyfluorescencepolarization
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