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On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench

We developed optically driven microtools for processing single biomolecules using a microfluidic workbench composed of a microfluidic platform that functions under an optical microscope. The optically driven microtools have enzymes immobilized on their surfaces, which catalyze chemical reactions for...

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Autores principales: Masuda, Akihito, Takao, Hidekuni, Shimokawa, Fusao, Terao, Kyohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042024/
https://www.ncbi.nlm.nih.gov/pubmed/33846479
http://dx.doi.org/10.1038/s41598-021-87238-3
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author Masuda, Akihito
Takao, Hidekuni
Shimokawa, Fusao
Terao, Kyohei
author_facet Masuda, Akihito
Takao, Hidekuni
Shimokawa, Fusao
Terao, Kyohei
author_sort Masuda, Akihito
collection PubMed
description We developed optically driven microtools for processing single biomolecules using a microfluidic workbench composed of a microfluidic platform that functions under an optical microscope. The optically driven microtools have enzymes immobilized on their surfaces, which catalyze chemical reactions for molecular processing in a confined space. Optical manipulation of the microtools enables them to be integrated with a microfluidic device for controlling the position, orientation, shape of the target sample. Here, we describe the immobilization of enzymes on the surface of microtools, the microfluidics workbench, including its microtool storage and sample positioning functions, and the use of this system for on-site cutting of single chromosomal DNA molecules. We fabricated microtools by UV lithography with SU-8 and selected ozone treatments for immobilizing enzymes. The microfluidic workbench has tool-stock chambers for tool storage and micropillars to trap and extend single chromosomal DNA molecules. The DNA cutting enzymes DNaseI and DNaseII were immobilized on microtools that were manipulated using optical tweezers. The DNaseI tool shows reliable cutting for on-site processing. This pinpoint processing provides an approach for analyzing chromosomal DNA at the single-molecule level. The flexibility of the microtool design allows for processing of various samples, including biomolecules and single cells.
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spelling pubmed-80420242021-04-14 On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench Masuda, Akihito Takao, Hidekuni Shimokawa, Fusao Terao, Kyohei Sci Rep Article We developed optically driven microtools for processing single biomolecules using a microfluidic workbench composed of a microfluidic platform that functions under an optical microscope. The optically driven microtools have enzymes immobilized on their surfaces, which catalyze chemical reactions for molecular processing in a confined space. Optical manipulation of the microtools enables them to be integrated with a microfluidic device for controlling the position, orientation, shape of the target sample. Here, we describe the immobilization of enzymes on the surface of microtools, the microfluidics workbench, including its microtool storage and sample positioning functions, and the use of this system for on-site cutting of single chromosomal DNA molecules. We fabricated microtools by UV lithography with SU-8 and selected ozone treatments for immobilizing enzymes. The microfluidic workbench has tool-stock chambers for tool storage and micropillars to trap and extend single chromosomal DNA molecules. The DNA cutting enzymes DNaseI and DNaseII were immobilized on microtools that were manipulated using optical tweezers. The DNaseI tool shows reliable cutting for on-site processing. This pinpoint processing provides an approach for analyzing chromosomal DNA at the single-molecule level. The flexibility of the microtool design allows for processing of various samples, including biomolecules and single cells. Nature Publishing Group UK 2021-04-12 /pmc/articles/PMC8042024/ /pubmed/33846479 http://dx.doi.org/10.1038/s41598-021-87238-3 Text en © The Author(s) 2021 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
Masuda, Akihito
Takao, Hidekuni
Shimokawa, Fusao
Terao, Kyohei
On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench
title On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench
title_full On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench
title_fullStr On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench
title_full_unstemmed On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench
title_short On-site processing of single chromosomal DNA molecules using optically driven microtools on a microfluidic workbench
title_sort on-site processing of single chromosomal dna molecules using optically driven microtools on a microfluidic workbench
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042024/
https://www.ncbi.nlm.nih.gov/pubmed/33846479
http://dx.doi.org/10.1038/s41598-021-87238-3
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