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Acoustofluidic Chemical Waveform Generator and Switch
[Image: see text] Eliciting a cellular response to a changing chemical microenvironment is central to many biological processes including gene expression, cell migration, differentiation, apoptosis, and intercellular signaling. The nature and scope of the response is highly dependent upon the spatio...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255676/ https://www.ncbi.nlm.nih.gov/pubmed/25405550 http://dx.doi.org/10.1021/ac5033676 |
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author | Ahmed, Daniel Muddana, Hari S. Lu, Mengqian French, Jarrod B. Ozcelik, Adem Fang, Ye Butler, Peter J. Benkovic, Stephen J. Manz, Andreas Huang, Tony Jun |
author_facet | Ahmed, Daniel Muddana, Hari S. Lu, Mengqian French, Jarrod B. Ozcelik, Adem Fang, Ye Butler, Peter J. Benkovic, Stephen J. Manz, Andreas Huang, Tony Jun |
author_sort | Ahmed, Daniel |
collection | PubMed |
description | [Image: see text] Eliciting a cellular response to a changing chemical microenvironment is central to many biological processes including gene expression, cell migration, differentiation, apoptosis, and intercellular signaling. The nature and scope of the response is highly dependent upon the spatiotemporal characteristics of the stimulus. To date, studies that investigate this phenomenon have been limited to digital (or step) chemical stimulation with little control over the temporal counterparts. Here, we demonstrate an acoustofluidic (i.e., fusion of acoustics and microfluidics) approach for generating programmable chemical waveforms that permits continuous modulation of the signal characteristics including the amplitude (i.e., sample concentration), shape, frequency, and duty cycle, with frequencies reaching up to 30 Hz. Furthermore, we show fast switching between multiple distinct stimuli, wherein the waveform of each stimulus is independently controlled. Using our device, we characterized the frequency-dependent activation and internalization of the β(2)-adrenergic receptor (β(2)-AR), a prototypic G-protein coupled receptor (GPCR), using epinephrine. The acoustofluidic-based programmable chemical waveform generation and switching method presented herein is expected to be a powerful tool for the investigation and characterization of the kinetics and other dynamic properties of many biological and biochemical processes. |
format | Online Article Text |
id | pubmed-4255676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42556762015-11-18 Acoustofluidic Chemical Waveform Generator and Switch Ahmed, Daniel Muddana, Hari S. Lu, Mengqian French, Jarrod B. Ozcelik, Adem Fang, Ye Butler, Peter J. Benkovic, Stephen J. Manz, Andreas Huang, Tony Jun Anal Chem [Image: see text] Eliciting a cellular response to a changing chemical microenvironment is central to many biological processes including gene expression, cell migration, differentiation, apoptosis, and intercellular signaling. The nature and scope of the response is highly dependent upon the spatiotemporal characteristics of the stimulus. To date, studies that investigate this phenomenon have been limited to digital (or step) chemical stimulation with little control over the temporal counterparts. Here, we demonstrate an acoustofluidic (i.e., fusion of acoustics and microfluidics) approach for generating programmable chemical waveforms that permits continuous modulation of the signal characteristics including the amplitude (i.e., sample concentration), shape, frequency, and duty cycle, with frequencies reaching up to 30 Hz. Furthermore, we show fast switching between multiple distinct stimuli, wherein the waveform of each stimulus is independently controlled. Using our device, we characterized the frequency-dependent activation and internalization of the β(2)-adrenergic receptor (β(2)-AR), a prototypic G-protein coupled receptor (GPCR), using epinephrine. The acoustofluidic-based programmable chemical waveform generation and switching method presented herein is expected to be a powerful tool for the investigation and characterization of the kinetics and other dynamic properties of many biological and biochemical processes. American Chemical Society 2014-11-18 2014-12-02 /pmc/articles/PMC4255676/ /pubmed/25405550 http://dx.doi.org/10.1021/ac5033676 Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Ahmed, Daniel Muddana, Hari S. Lu, Mengqian French, Jarrod B. Ozcelik, Adem Fang, Ye Butler, Peter J. Benkovic, Stephen J. Manz, Andreas Huang, Tony Jun Acoustofluidic Chemical Waveform Generator and Switch |
title | Acoustofluidic Chemical Waveform Generator and Switch |
title_full | Acoustofluidic Chemical Waveform Generator and Switch |
title_fullStr | Acoustofluidic Chemical Waveform Generator and Switch |
title_full_unstemmed | Acoustofluidic Chemical Waveform Generator and Switch |
title_short | Acoustofluidic Chemical Waveform Generator and Switch |
title_sort | acoustofluidic chemical waveform generator and switch |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255676/ https://www.ncbi.nlm.nih.gov/pubmed/25405550 http://dx.doi.org/10.1021/ac5033676 |
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