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A microfluidic platform for trapping, releasing and super-resolution imaging of single cells
A multi-layer device, combining hydrodynamic trapping with microfluidic valving techniques, has been developed for on-chip manipulation and imaging of single cells and particles. Such a device contains a flow layer with trapping channels to capture single particles or cells and a control layer with...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Sequoia
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872524/ https://www.ncbi.nlm.nih.gov/pubmed/27594767 http://dx.doi.org/10.1016/j.snb.2016.03.131 |
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author | Zhou, Ying Basu, Srinjan Wohlfahrt, Kai J. Lee, Steven F. Klenerman, David Laue, Ernest D. Seshia, Ashwin A. |
author_facet | Zhou, Ying Basu, Srinjan Wohlfahrt, Kai J. Lee, Steven F. Klenerman, David Laue, Ernest D. Seshia, Ashwin A. |
author_sort | Zhou, Ying |
collection | PubMed |
description | A multi-layer device, combining hydrodynamic trapping with microfluidic valving techniques, has been developed for on-chip manipulation and imaging of single cells and particles. Such a device contains a flow layer with trapping channels to capture single particles or cells and a control layer with valve channels to selectively control the trap and release processes. Particles and cells have been successfully trapped and released using the proposed device. The device enables the trapping of single particles with a trapping efficiency of greater than 95%, and allows for single particles and cells to be trapped, released and manipulated by simply controlling corresponding valves. Moreover, the trap and release processes are found to be compatible with biological samples like cells. Our device allows stable immobilisation of large numbers of single cells in a few minutes, significantly easing the experiment setup for single-cell characterisation and offering a stable platform for both single-molecule and super-resolution imaging. Proof-of-concept super- resolution imaging experiments with mouse embryonic stem cells (mESCs) have been conducted by exploiting super-resolution photoactivated localisation microscopy (PALM). Cells and nuclei were stably trapped and imaged. Centromeres of ∼200 nm size could be identified with a localisation precision of <15 nm. |
format | Online Article Text |
id | pubmed-4872524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier Sequoia |
record_format | MEDLINE/PubMed |
spelling | pubmed-48725242016-09-01 A microfluidic platform for trapping, releasing and super-resolution imaging of single cells Zhou, Ying Basu, Srinjan Wohlfahrt, Kai J. Lee, Steven F. Klenerman, David Laue, Ernest D. Seshia, Ashwin A. Sens Actuators B Chem Article A multi-layer device, combining hydrodynamic trapping with microfluidic valving techniques, has been developed for on-chip manipulation and imaging of single cells and particles. Such a device contains a flow layer with trapping channels to capture single particles or cells and a control layer with valve channels to selectively control the trap and release processes. Particles and cells have been successfully trapped and released using the proposed device. The device enables the trapping of single particles with a trapping efficiency of greater than 95%, and allows for single particles and cells to be trapped, released and manipulated by simply controlling corresponding valves. Moreover, the trap and release processes are found to be compatible with biological samples like cells. Our device allows stable immobilisation of large numbers of single cells in a few minutes, significantly easing the experiment setup for single-cell characterisation and offering a stable platform for both single-molecule and super-resolution imaging. Proof-of-concept super- resolution imaging experiments with mouse embryonic stem cells (mESCs) have been conducted by exploiting super-resolution photoactivated localisation microscopy (PALM). Cells and nuclei were stably trapped and imaged. Centromeres of ∼200 nm size could be identified with a localisation precision of <15 nm. Elsevier Sequoia 2016-09 /pmc/articles/PMC4872524/ /pubmed/27594767 http://dx.doi.org/10.1016/j.snb.2016.03.131 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Zhou, Ying Basu, Srinjan Wohlfahrt, Kai J. Lee, Steven F. Klenerman, David Laue, Ernest D. Seshia, Ashwin A. A microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
title | A microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
title_full | A microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
title_fullStr | A microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
title_full_unstemmed | A microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
title_short | A microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
title_sort | microfluidic platform for trapping, releasing and super-resolution imaging of single cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872524/ https://www.ncbi.nlm.nih.gov/pubmed/27594767 http://dx.doi.org/10.1016/j.snb.2016.03.131 |
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