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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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 |
work_keys_str_mv |
AT anushakeloth singlecellisolationusingopticaltweezers AT owenanderson singlecellisolationusingopticaltweezers AT donaldrisbridger singlecellisolationusingopticaltweezers AT lynnpaterson singlecellisolationusingopticaltweezers |
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