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Using dielectrophoresis to study the dynamic response of single budding yeast cells to Lyticase

Using dielectrophoresis to study the dynamic response of single budding yeast cells to Lyticase
Using dielectrophoresis to study the dynamic response of single budding yeast cells to Lyticase

Budding yeast cells are quick and easy to grow and represent a versatile model of eukaryotic cells for a variety of cellular studies, largely because their genome has been widely studied and links can be drawn with higher eukaryotes. Therefore, the efficient separation, immobilization, and conversion of budding yeasts into spheroplast or protoplast can provide valuable insight for many fundamentals investigations in cell biology at a single cell level. Dielectrophoresis, the induced motion of particles in non-uniform electric fields, possesses a great versatility for manipulation of cells in microfluidic platforms. Despite this, dielectrophoresis has been largely utilized for studying of non-budding yeast cells and has rarely been used for manipulation of budding cells. Here, we utilize dielectrophoresis for studying the dynamic response of budding cells to different concentrations of Lyticase. This involves separation of the budding yeasts from a background of non-budding cells and their subsequent immobilization onto the microelectrodes at desired densities down to single cell level. The immobilized yeasts are then stimulated with Lyticase to remove the cell wall and convert them into spheroplasts, in a highly dynamic process that depends on the concentration of Lyticase. We also introduce a novel method for immobilization of the cell organelles released from the lysed cells by patterning multi-walled carbon nanotubes (MWCNTs) between the microelectrodes.

Dielectrophoresis, Microfluidics, Yeast
1618-2642
Tang, Shi Yang
1d0f15c6-2a3e-4bad-a3d8-fc267db93ed4
Yi, Pyshar
497e4f29-d085-4011-b8fa-19d515591f6d
Soffe, Rebecca
c1670df9-4ac4-4abc-8c48-3f6048a4e9fb
Nahavandi, Sofia
93efa445-8eac-4999-9204-969a014bb717
Shukla, Ravi
cb4cdadb-63cc-482e-8f41-2974f0a0f70a
Khoshmanesh, Khashayar
72608a1e-0e41-4360-8065-98d872493aed
Tang, Shi Yang
1d0f15c6-2a3e-4bad-a3d8-fc267db93ed4
Yi, Pyshar
497e4f29-d085-4011-b8fa-19d515591f6d
Soffe, Rebecca
c1670df9-4ac4-4abc-8c48-3f6048a4e9fb
Nahavandi, Sofia
93efa445-8eac-4999-9204-969a014bb717
Shukla, Ravi
cb4cdadb-63cc-482e-8f41-2974f0a0f70a
Khoshmanesh, Khashayar
72608a1e-0e41-4360-8065-98d872493aed

Tang, Shi Yang, Yi, Pyshar, Soffe, Rebecca, Nahavandi, Sofia, Shukla, Ravi and Khoshmanesh, Khashayar (2015) Using dielectrophoresis to study the dynamic response of single budding yeast cells to Lyticase. Analytical and Bioanalytical Chemistry, 407 (12). (doi:10.1007/s00216-015-8529-1). (In Press)

Record type: Article

Abstract

Budding yeast cells are quick and easy to grow and represent a versatile model of eukaryotic cells for a variety of cellular studies, largely because their genome has been widely studied and links can be drawn with higher eukaryotes. Therefore, the efficient separation, immobilization, and conversion of budding yeasts into spheroplast or protoplast can provide valuable insight for many fundamentals investigations in cell biology at a single cell level. Dielectrophoresis, the induced motion of particles in non-uniform electric fields, possesses a great versatility for manipulation of cells in microfluidic platforms. Despite this, dielectrophoresis has been largely utilized for studying of non-budding yeast cells and has rarely been used for manipulation of budding cells. Here, we utilize dielectrophoresis for studying the dynamic response of budding cells to different concentrations of Lyticase. This involves separation of the budding yeasts from a background of non-budding cells and their subsequent immobilization onto the microelectrodes at desired densities down to single cell level. The immobilized yeasts are then stimulated with Lyticase to remove the cell wall and convert them into spheroplasts, in a highly dynamic process that depends on the concentration of Lyticase. We also introduce a novel method for immobilization of the cell organelles released from the lysed cells by patterning multi-walled carbon nanotubes (MWCNTs) between the microelectrodes.

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More information

Accepted/In Press date: 21 February 2015
Additional Information: Funding Information: K. Khoshmanesh acknowledges the Australian Research Council for funding under Discovery Early Career Researcher Award (DECRA) scheme (project DE120101402). R. Shukla thanks RMIT University for VC Research Fellowship. Publisher Copyright: © 2015 Springer-Verlag Berlin Heidelberg
Keywords: Dielectrophoresis, Microfluidics, Yeast

Identifiers

Local EPrints ID: 481671
URI: http://eprints.soton.ac.uk/id/eprint/481671
ISSN: 1618-2642
PURE UUID: 9861ae4d-141a-4b38-bf4e-c7818b6187e8
ORCID for Shi Yang Tang: ORCID iD orcid.org/0000-0002-3079-8880

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Date deposited: 05 Sep 2023 16:57
Last modified: 18 Mar 2024 04:13

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Contributors

Author: Shi Yang Tang ORCID iD
Author: Pyshar Yi
Author: Rebecca Soffe
Author: Sofia Nahavandi
Author: Ravi Shukla
Author: Khashayar Khoshmanesh

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