Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.

We developed an active virus filter (AVF) that enables virus enrichment for single virus infection, by using insulator-based dielectrophoresis (iDEP). A 3D-constricted flow channel design enabled the production of an iDEP force in the microfluidic chip. iDEP using a chip with multiple active virus f...

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Main Authors: Taisuke Masuda, Hisataka Maruyama, Ayae Honda, Fumihito Arai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4053322?pdf=render
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spelling doaj-d84e901af4da4d3099d317e1fb32f27d2020-11-25T01:12:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e9408310.1371/journal.pone.0094083Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.Taisuke MasudaHisataka MaruyamaAyae HondaFumihito AraiWe developed an active virus filter (AVF) that enables virus enrichment for single virus infection, by using insulator-based dielectrophoresis (iDEP). A 3D-constricted flow channel design enabled the production of an iDEP force in the microfluidic chip. iDEP using a chip with multiple active virus filters (AVFs) was more accurate and faster than using a chip with a single AVF, and improved the efficiency of virus trapping. We utilized maskless photolithography to achieve the precise 3D gray-scale exposure required for fabrication of constricted flow channel. Influenza virus (A PR/8) was enriched by a negative DEP force when sinusoidal wave was applied to the electrodes within an amplitude range of 20 Vp-p and a frequency of 10 MHz. AVF-mediated virus enrichment can be repeated simply by turning the current ON or OFF. Furthermore, the negative AVF can inhibit virus adhesion onto the glass substrate. We then trapped and transported one of the enriched viruses by using optical tweezers. This microfluidic chip facilitated the effective transport of a single virus from AVFs towards the cell-containing chamber without crossing an electrode. We successfully transported the virus to the cell chamber (v = 10 µm/s) and brought it infected with a selected single H292 cell.http://europepmc.org/articles/PMC4053322?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Taisuke Masuda
Hisataka Maruyama
Ayae Honda
Fumihito Arai
spellingShingle Taisuke Masuda
Hisataka Maruyama
Ayae Honda
Fumihito Arai
Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.
PLoS ONE
author_facet Taisuke Masuda
Hisataka Maruyama
Ayae Honda
Fumihito Arai
author_sort Taisuke Masuda
title Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.
title_short Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.
title_full Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.
title_fullStr Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.
title_full_unstemmed Virus enrichment for single virus infection by using 3D insulator based dielectrophoresis.
title_sort virus enrichment for single virus infection by using 3d insulator based dielectrophoresis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description We developed an active virus filter (AVF) that enables virus enrichment for single virus infection, by using insulator-based dielectrophoresis (iDEP). A 3D-constricted flow channel design enabled the production of an iDEP force in the microfluidic chip. iDEP using a chip with multiple active virus filters (AVFs) was more accurate and faster than using a chip with a single AVF, and improved the efficiency of virus trapping. We utilized maskless photolithography to achieve the precise 3D gray-scale exposure required for fabrication of constricted flow channel. Influenza virus (A PR/8) was enriched by a negative DEP force when sinusoidal wave was applied to the electrodes within an amplitude range of 20 Vp-p and a frequency of 10 MHz. AVF-mediated virus enrichment can be repeated simply by turning the current ON or OFF. Furthermore, the negative AVF can inhibit virus adhesion onto the glass substrate. We then trapped and transported one of the enriched viruses by using optical tweezers. This microfluidic chip facilitated the effective transport of a single virus from AVFs towards the cell-containing chamber without crossing an electrode. We successfully transported the virus to the cell chamber (v = 10 µm/s) and brought it infected with a selected single H292 cell.
url http://europepmc.org/articles/PMC4053322?pdf=render
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