Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria

Microfluidics has become an essential tool in single-cell analysis assays for gaining more accurate insights into cell behavior. Various microfluidics methods have been introduced facilitating single-cell analysis of a broad range of cell types. However, the study of prokaryotic cells such as Escher...

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Main Authors: Dietrich Kohlheyer, Christopher Probst, Wolfgang Wiechert, Alexander Grünberger
Format: Article
Language:English
Published: MDPI AG 2013-10-01
Series:Micromachines
Subjects:
Online Access:http://www.mdpi.com/2072-666X/4/4/357
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spelling doaj-9409fc3c873449f1a639c816bcf008e12020-11-24T23:08:26ZengMDPI AGMicromachines2072-666X2013-10-014435736910.3390/mi4040357Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of BacteriaDietrich KohlheyerChristopher ProbstWolfgang WiechertAlexander GrünbergerMicrofluidics has become an essential tool in single-cell analysis assays for gaining more accurate insights into cell behavior. Various microfluidics methods have been introduced facilitating single-cell analysis of a broad range of cell types. However, the study of prokaryotic cells such as Escherichia coli and others still faces the challenge of achieving proper single-cell immobilization simply due to their small size and often fast growth rates. Recently, new approaches were presented to investigate bacteria growing in monolayers and single-cell tracks under environmental control. This allows for high-resolution time-lapse observation of cell proliferation, cell morphology and fluorescence-coupled bioreporters. Inside microcolonies, interactions between nearby cells are likely and may cause interference during perturbation studies. In this paper, we present a microfluidic device containing hundred sub-micron sized trapping barrier structures for single E. coli cells. Descendant cells are rapidly washed away as well as components secreted by growing cells. Experiments show excellent growth rates, indicating high cell viability. Analyses of elongation and growth rates as well as morphology were successfully performed. This device will find application in prokaryotic single-cell studies under constant environment where by-product interference is undesired.http://www.mdpi.com/2072-666X/4/4/357microfluidicssingle-cell analysisE. colibacteria
collection DOAJ
language English
format Article
sources DOAJ
author Dietrich Kohlheyer
Christopher Probst
Wolfgang Wiechert
Alexander Grünberger
spellingShingle Dietrich Kohlheyer
Christopher Probst
Wolfgang Wiechert
Alexander Grünberger
Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
Micromachines
microfluidics
single-cell analysis
E. coli
bacteria
author_facet Dietrich Kohlheyer
Christopher Probst
Wolfgang Wiechert
Alexander Grünberger
author_sort Dietrich Kohlheyer
title Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
title_short Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
title_full Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
title_fullStr Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
title_full_unstemmed Polydimethylsiloxane (PDMS) Sub-Micron Traps for Single-Cell Analysis of Bacteria
title_sort polydimethylsiloxane (pdms) sub-micron traps for single-cell analysis of bacteria
publisher MDPI AG
series Micromachines
issn 2072-666X
publishDate 2013-10-01
description Microfluidics has become an essential tool in single-cell analysis assays for gaining more accurate insights into cell behavior. Various microfluidics methods have been introduced facilitating single-cell analysis of a broad range of cell types. However, the study of prokaryotic cells such as Escherichia coli and others still faces the challenge of achieving proper single-cell immobilization simply due to their small size and often fast growth rates. Recently, new approaches were presented to investigate bacteria growing in monolayers and single-cell tracks under environmental control. This allows for high-resolution time-lapse observation of cell proliferation, cell morphology and fluorescence-coupled bioreporters. Inside microcolonies, interactions between nearby cells are likely and may cause interference during perturbation studies. In this paper, we present a microfluidic device containing hundred sub-micron sized trapping barrier structures for single E. coli cells. Descendant cells are rapidly washed away as well as components secreted by growing cells. Experiments show excellent growth rates, indicating high cell viability. Analyses of elongation and growth rates as well as morphology were successfully performed. This device will find application in prokaryotic single-cell studies under constant environment where by-product interference is undesired.
topic microfluidics
single-cell analysis
E. coli
bacteria
url http://www.mdpi.com/2072-666X/4/4/357
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