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A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition

[Image: see text] The ability to miniaturize biochemical assays in water-in-oil emulsion droplets allows a massive scale-down of reaction volumes, so that high-throughput experimentation can be performed more economically and more efficiently. Generating such droplets in compartment-on-demand (COD)...

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Autores principales: Gielen, Fabrice, van Vliet, Liisa, Koprowski, Bartosz T., Devenish, Sean R. A., Fischlechner, Martin, Edel, Joshua B., Niu, Xize, deMello, Andrew J., Hollfelder, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715888/
https://www.ncbi.nlm.nih.gov/pubmed/23614771
http://dx.doi.org/10.1021/ac400480z
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author Gielen, Fabrice
van Vliet, Liisa
Koprowski, Bartosz T.
Devenish, Sean R. A.
Fischlechner, Martin
Edel, Joshua B.
Niu, Xize
deMello, Andrew J.
Hollfelder, Florian
author_facet Gielen, Fabrice
van Vliet, Liisa
Koprowski, Bartosz T.
Devenish, Sean R. A.
Fischlechner, Martin
Edel, Joshua B.
Niu, Xize
deMello, Andrew J.
Hollfelder, Florian
author_sort Gielen, Fabrice
collection PubMed
description [Image: see text] The ability to miniaturize biochemical assays in water-in-oil emulsion droplets allows a massive scale-down of reaction volumes, so that high-throughput experimentation can be performed more economically and more efficiently. Generating such droplets in compartment-on-demand (COD) platforms is the basis for rapid, automated screening of chemical and biological libraries with minimal volume consumption. Herein, we describe the implementation of such a COD platform to perform high precision nanoliter assays. The coupling of a COD platform to a droplet absorbance detection set-up results in a fully automated analytical system. Michaelis–Menten parameters of 4-nitrophenyl glucopyranoside hydrolysis by sweet almond β-glucosidase can be generated based on 24 time-courses taken at different substrate concentrations with a total volume consumption of only 1.4 μL. Importantly, kinetic parameters can be derived in a fully unsupervised manner within 20 min: droplet production (5 min), initial reading of the droplet sequence (5 min), and droplet fusion to initiate the reaction and read-out over time (10 min). Similarly, the inhibition of the enzymatic reaction by conduritol B epoxide and 1-deoxynojirimycin was measured, and K(i) values were determined. In both cases, the kinetic parameters obtained in droplets were identical within error to values obtained in titer plates, despite a >10(4)-fold volume reduction, from micro- to nanoliters.
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spelling pubmed-37158882013-07-19 A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition Gielen, Fabrice van Vliet, Liisa Koprowski, Bartosz T. Devenish, Sean R. A. Fischlechner, Martin Edel, Joshua B. Niu, Xize deMello, Andrew J. Hollfelder, Florian Anal Chem [Image: see text] The ability to miniaturize biochemical assays in water-in-oil emulsion droplets allows a massive scale-down of reaction volumes, so that high-throughput experimentation can be performed more economically and more efficiently. Generating such droplets in compartment-on-demand (COD) platforms is the basis for rapid, automated screening of chemical and biological libraries with minimal volume consumption. Herein, we describe the implementation of such a COD platform to perform high precision nanoliter assays. The coupling of a COD platform to a droplet absorbance detection set-up results in a fully automated analytical system. Michaelis–Menten parameters of 4-nitrophenyl glucopyranoside hydrolysis by sweet almond β-glucosidase can be generated based on 24 time-courses taken at different substrate concentrations with a total volume consumption of only 1.4 μL. Importantly, kinetic parameters can be derived in a fully unsupervised manner within 20 min: droplet production (5 min), initial reading of the droplet sequence (5 min), and droplet fusion to initiate the reaction and read-out over time (10 min). Similarly, the inhibition of the enzymatic reaction by conduritol B epoxide and 1-deoxynojirimycin was measured, and K(i) values were determined. In both cases, the kinetic parameters obtained in droplets were identical within error to values obtained in titer plates, despite a >10(4)-fold volume reduction, from micro- to nanoliters. American Chemical Society 2013-04-03 2013-05-07 /pmc/articles/PMC3715888/ /pubmed/23614771 http://dx.doi.org/10.1021/ac400480z Text en Copyright © 2013 American Chemical Society Terms of Use CC-BY (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html)
spellingShingle Gielen, Fabrice
van Vliet, Liisa
Koprowski, Bartosz T.
Devenish, Sean R. A.
Fischlechner, Martin
Edel, Joshua B.
Niu, Xize
deMello, Andrew J.
Hollfelder, Florian
A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition
title A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition
title_full A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition
title_fullStr A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition
title_full_unstemmed A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition
title_short A Fully Unsupervised Compartment-on-Demand Platform for Precise Nanoliter Assays of Time-Dependent Steady-State Enzyme Kinetics and Inhibition
title_sort fully unsupervised compartment-on-demand platform for precise nanoliter assays of time-dependent steady-state enzyme kinetics and inhibition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3715888/
https://www.ncbi.nlm.nih.gov/pubmed/23614771
http://dx.doi.org/10.1021/ac400480z
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