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Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip

We report analysis of phosphatase activity and inhibition on droplet-based microfluidic chips. Phosphatases are such attractive potential drug targets because abnormal phosphatase activity has been implicated in a variety of diseases including cancer, neurological disorders, diabetes, osteoporosis,...

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Autores principales: Vasamsetti, Bala Murali Krishna, Kim, Yeon-Jun, Kang, Jung Hoon, Choi, Jae-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496282/
https://www.ncbi.nlm.nih.gov/pubmed/36140125
http://dx.doi.org/10.3390/bios12090740
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author Vasamsetti, Bala Murali Krishna
Kim, Yeon-Jun
Kang, Jung Hoon
Choi, Jae-Won
author_facet Vasamsetti, Bala Murali Krishna
Kim, Yeon-Jun
Kang, Jung Hoon
Choi, Jae-Won
author_sort Vasamsetti, Bala Murali Krishna
collection PubMed
description We report analysis of phosphatase activity and inhibition on droplet-based microfluidic chips. Phosphatases are such attractive potential drug targets because abnormal phosphatase activity has been implicated in a variety of diseases including cancer, neurological disorders, diabetes, osteoporosis, and obesity. So far, several methods for assessing phosphatase activity have been reported. However, they require a large sample volume and additional chemical modifications such as fluorescent dye conjugation and nanomaterial conjugation, and are not cost-effective. In this study, we used an artificial phosphatase substrate 3-O-methylfluorescein phosphate as a fluorescent reporter and dual specificity phosphatase 22. Using these materials, the phosphatase assay was performed from approximately 340.4 picoliter (pL) droplets generated at a frequency of ~40 hertz (Hz) in a droplet-based microfluidic chip. To evaluate the suitability of droplet-based platform for screening phosphatase inhibitors, a dose–response inhibition study was performed with ethyl-3,4-dephostatin and the half-maximal inhibitory concentration (IC(50)) was calculated as 5.79 ± 1.09 μM. The droplet-based results were compared to microplate-based experiments, which showed agreement. The droplet-based phosphatase assay proposed here is simple, reproducible, and generates enormous data sets within the limited sample and reagent volumes.
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spelling pubmed-94962822022-09-23 Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip Vasamsetti, Bala Murali Krishna Kim, Yeon-Jun Kang, Jung Hoon Choi, Jae-Won Biosensors (Basel) Article We report analysis of phosphatase activity and inhibition on droplet-based microfluidic chips. Phosphatases are such attractive potential drug targets because abnormal phosphatase activity has been implicated in a variety of diseases including cancer, neurological disorders, diabetes, osteoporosis, and obesity. So far, several methods for assessing phosphatase activity have been reported. However, they require a large sample volume and additional chemical modifications such as fluorescent dye conjugation and nanomaterial conjugation, and are not cost-effective. In this study, we used an artificial phosphatase substrate 3-O-methylfluorescein phosphate as a fluorescent reporter and dual specificity phosphatase 22. Using these materials, the phosphatase assay was performed from approximately 340.4 picoliter (pL) droplets generated at a frequency of ~40 hertz (Hz) in a droplet-based microfluidic chip. To evaluate the suitability of droplet-based platform for screening phosphatase inhibitors, a dose–response inhibition study was performed with ethyl-3,4-dephostatin and the half-maximal inhibitory concentration (IC(50)) was calculated as 5.79 ± 1.09 μM. The droplet-based results were compared to microplate-based experiments, which showed agreement. The droplet-based phosphatase assay proposed here is simple, reproducible, and generates enormous data sets within the limited sample and reagent volumes. MDPI 2022-09-08 /pmc/articles/PMC9496282/ /pubmed/36140125 http://dx.doi.org/10.3390/bios12090740 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vasamsetti, Bala Murali Krishna
Kim, Yeon-Jun
Kang, Jung Hoon
Choi, Jae-Won
Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip
title Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip
title_full Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip
title_fullStr Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip
title_full_unstemmed Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip
title_short Analysis of Phosphatase Activity in a Droplet-Based Microfluidic Chip
title_sort analysis of phosphatase activity in a droplet-based microfluidic chip
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496282/
https://www.ncbi.nlm.nih.gov/pubmed/36140125
http://dx.doi.org/10.3390/bios12090740
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