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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)...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2013
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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. |
format | Online Article Text |
id | pubmed-3715888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
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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