Single Cell Isolation Using Optical Tweezers

Optical tweezers offer a non-contact method for selecting single cells and translocating them from one microenvironment to another. We have characterized the optical tweezing of yeast S. cerevisiae and can manipulate single cells at 0.41 ± 0.06 mm/s using a 26.8 ± 0.1 mW from a...

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Main Authors: Anusha Keloth, Owen Anderson, Donald Risbridger, Lynn Paterson
Format: Article
Language:English
Published: MDPI AG 2018-08-01
Series:Micromachines
Subjects:
Online Access:http://www.mdpi.com/2072-666X/9/9/434
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spelling doaj-d148b58127f342bc8cd19cd65e86e64b2020-11-25T02:29:15ZengMDPI AGMicromachines2072-666X2018-08-019943410.3390/mi9090434mi9090434Single Cell Isolation Using Optical TweezersAnusha Keloth0Owen Anderson1Donald Risbridger2Lynn Paterson3Institute of Biological Chemistry, Biophysics and Bioengineering, School of Engineering and Physical Sciences, Heriot Watt University, Edinburgh EH14 4AS, UKInstitute of Biological Chemistry, Biophysics and Bioengineering, School of Engineering and Physical Sciences, Heriot Watt University, Edinburgh EH14 4AS, UKInstitute of Biological Chemistry, Biophysics and Bioengineering, School of Engineering and Physical Sciences, Heriot Watt University, Edinburgh EH14 4AS, UKInstitute of Biological Chemistry, Biophysics and Bioengineering, School of Engineering and Physical Sciences, Heriot Watt University, Edinburgh EH14 4AS, UKOptical tweezers offer a non-contact method for selecting single cells and translocating them from one microenvironment to another. We have characterized the optical tweezing of yeast S. cerevisiae and can manipulate single cells at 0.41 ± 0.06 mm/s using a 26.8 ± 0.1 mW from a 785 nm diode laser. We have fabricated and tested three cell isolation devices; a micropipette, a PDMS chip and a laser machined fused silica chip and we have isolated yeast, single bacteria and cyanobacteria cells. The most effective isolation was achieved in PDMS chips, where single yeast cells were grown and observed for 18 h without contamination. The duration of budding in S. cerevisiae was not affected by the laser parameters used, but the time from tweezing until the first budding event began increased with increasing laser energy (laser power × time). Yeast cells tweezed using 25.0 ± 0.1 mW for 1 min were viable after isolation. We have constructed a micro-consortium of yeast cells, and a co-culture of yeast and bacteria, using optical tweezers in combination with the PDMS network of channels and isolation chambers, which may impact on both industrial biotechnology and understanding pathogen dynamics.http://www.mdpi.com/2072-666X/9/9/434optical tweezersoptical trapPDMS devicessingle cells
collection DOAJ
language English
format Article
sources DOAJ
author Anusha Keloth
Owen Anderson
Donald Risbridger
Lynn Paterson
spellingShingle Anusha Keloth
Owen Anderson
Donald Risbridger
Lynn Paterson
Single Cell Isolation Using Optical Tweezers
Micromachines
optical tweezers
optical trap
PDMS devices
single cells
author_facet Anusha Keloth
Owen Anderson
Donald Risbridger
Lynn Paterson
author_sort Anusha Keloth
title Single Cell Isolation Using Optical Tweezers
title_short Single Cell Isolation Using Optical Tweezers
title_full Single Cell Isolation Using Optical Tweezers
title_fullStr Single Cell Isolation Using Optical Tweezers
title_full_unstemmed Single Cell Isolation Using Optical Tweezers
title_sort single cell isolation using optical tweezers
publisher MDPI AG
series Micromachines
issn 2072-666X
publishDate 2018-08-01
description Optical tweezers offer a non-contact method for selecting single cells and translocating them from one microenvironment to another. We have characterized the optical tweezing of yeast S. cerevisiae and can manipulate single cells at 0.41 ± 0.06 mm/s using a 26.8 ± 0.1 mW from a 785 nm diode laser. We have fabricated and tested three cell isolation devices; a micropipette, a PDMS chip and a laser machined fused silica chip and we have isolated yeast, single bacteria and cyanobacteria cells. The most effective isolation was achieved in PDMS chips, where single yeast cells were grown and observed for 18 h without contamination. The duration of budding in S. cerevisiae was not affected by the laser parameters used, but the time from tweezing until the first budding event began increased with increasing laser energy (laser power × time). Yeast cells tweezed using 25.0 ± 0.1 mW for 1 min were viable after isolation. We have constructed a micro-consortium of yeast cells, and a co-culture of yeast and bacteria, using optical tweezers in combination with the PDMS network of channels and isolation chambers, which may impact on both industrial biotechnology and understanding pathogen dynamics.
topic optical tweezers
optical trap
PDMS devices
single cells
url http://www.mdpi.com/2072-666X/9/9/434
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