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Micro- and nanochamber array system for single enzyme assays

Arrays of small reaction containers, ranging from 624 femtoliters (10(–15) L) to 270 attoliters (10(–18) L), for capturing a single enzyme molecule and measuring the activity were developed along with a new reversible sealing system based on a pneumatic valve actuator made of polydimethylsiloxane (P...

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Autores principales: Iijima, Kazuki, Kaji, Noritada, Tokeshi, Manabu, Baba, Yoshinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432523/
https://www.ncbi.nlm.nih.gov/pubmed/37587179
http://dx.doi.org/10.1038/s41598-023-40544-4
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author Iijima, Kazuki
Kaji, Noritada
Tokeshi, Manabu
Baba, Yoshinobu
author_facet Iijima, Kazuki
Kaji, Noritada
Tokeshi, Manabu
Baba, Yoshinobu
author_sort Iijima, Kazuki
collection PubMed
description Arrays of small reaction containers, ranging from 624 femtoliters (10(–15) L) to 270 attoliters (10(–18) L), for capturing a single enzyme molecule and measuring the activity were developed along with a new reversible sealing system based on a pneumatic valve actuator made of polydimethylsiloxane (PDMS). The valve was actuated by PBS solution, effectively preventing evaporation of the solution from the micro- and nanochambers and allowing the assay to be performed over a long period of time. The hydrolysis rates of β-D-galactosidase (β-gal), k(cat), were decreased according to the decrease of the chamber size, and the overall tendency seems to be symmetrically related to the specific surface area of the chambers even under the prevented condition of non-specific adsorption. The spatial localization of the protons in the chambers, which might could affect the dissociation state of the proteins, was also investigated to explain the decrease in the hydrolysis rate. The developed chamber system developed here may be useful for artificially reproducing the confined intracellular environment and molecular crowding conditions.
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spelling pubmed-104325232023-08-18 Micro- and nanochamber array system for single enzyme assays Iijima, Kazuki Kaji, Noritada Tokeshi, Manabu Baba, Yoshinobu Sci Rep Article Arrays of small reaction containers, ranging from 624 femtoliters (10(–15) L) to 270 attoliters (10(–18) L), for capturing a single enzyme molecule and measuring the activity were developed along with a new reversible sealing system based on a pneumatic valve actuator made of polydimethylsiloxane (PDMS). The valve was actuated by PBS solution, effectively preventing evaporation of the solution from the micro- and nanochambers and allowing the assay to be performed over a long period of time. The hydrolysis rates of β-D-galactosidase (β-gal), k(cat), were decreased according to the decrease of the chamber size, and the overall tendency seems to be symmetrically related to the specific surface area of the chambers even under the prevented condition of non-specific adsorption. The spatial localization of the protons in the chambers, which might could affect the dissociation state of the proteins, was also investigated to explain the decrease in the hydrolysis rate. The developed chamber system developed here may be useful for artificially reproducing the confined intracellular environment and molecular crowding conditions. Nature Publishing Group UK 2023-08-16 /pmc/articles/PMC10432523/ /pubmed/37587179 http://dx.doi.org/10.1038/s41598-023-40544-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Iijima, Kazuki
Kaji, Noritada
Tokeshi, Manabu
Baba, Yoshinobu
Micro- and nanochamber array system for single enzyme assays
title Micro- and nanochamber array system for single enzyme assays
title_full Micro- and nanochamber array system for single enzyme assays
title_fullStr Micro- and nanochamber array system for single enzyme assays
title_full_unstemmed Micro- and nanochamber array system for single enzyme assays
title_short Micro- and nanochamber array system for single enzyme assays
title_sort micro- and nanochamber array system for single enzyme assays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432523/
https://www.ncbi.nlm.nih.gov/pubmed/37587179
http://dx.doi.org/10.1038/s41598-023-40544-4
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